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NCT Number: NCT05453019

Effects of CI on Tinnitus and Its Symptoms

Abnormal activity in the central auditory system is the cause of subjective experience of tinnitus. Electrical stimulation can inhibit the abnormal activity of auditory related neurons in patients with tinnitus. In recent years, the application of electrical stimulation in the treatment of tinnitus is a hot research topic, and has made some progress. However, its treatment is still in the discussion stage, and there is no best scheme suitable for clinical practice. At present, scholars have found that cochlear electrode stimulation can inhibit tinnitus, but its mechanism is not clear. It is difficult to locate the origin of tinnitus, and the location of electrode stimulation and stimulation parameters still need to be further optimized. Because the implanted part of the cochlear implant contains magnets, the patients cannot perform functional MRI. However, the prevalence of tinnitus in this group is very high (67.0~100.0%, with an average of 80.0%), so it is of great value and significance to study the effect of tinnitus treatment in such patients. In this study, a new clinical electroencephalogram (EEG) technique was used to make up for the lack of MRI imaging in patients with electrode implantation. EEG analyzes the functional connection of different brain regions through EEG test electrodes, uses the traceability function of EEG software to locate the location of tinnitus, analyzes the process of tinnitus inhibition by electrical stimulation, and explains the mechanism of tinnitus inhibition by electrical stimulation from a new perspective.

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Key information

Conditions

Tinnitus Ear Diseases Hearing Disorders Nervous System Diseases Neurologic Manifestations Otorhinolaryngologic Diseases Pathological Conditions, Signs and Symptoms Sensation Disorders Signs and Symptoms

Age range

16 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

  • Research content 1.1 Study on the change law of tinnitus affected by electrical stimulation after electrode implantation: 1) The change of tinnitus before operation after cochlear implantation; 2) Long term observation of electrical stimulation after cochlear implantation: (1) The change rule of tinnitus loudness after electrical stimulation (how long can it recover to be stable after power on); (2) The regularity of tinnitus frequency after electrical stimulation; (3) The recovery of tinnitus after electrode implantation for various causes of deafness.

1.2 Study on the mechanism of electric stimulation inhibiting tinnitus: 1) Changes of resting EEG in patients with tinnitus before surgery, before surgery-after surgery, 1 month, 2 months, 3 months, 6 months, 12 month, more than 12 months; 2) The compilation of resting electroencephalogram analysis program; 3) The resting brain wave shape was analyzed to trace the anatomical position of the artificial cochlea to inhibit tinnitus.

1.3 Study on the optimal setting of electrode stimulation for tinnitus treatment: 1) Setting different electric stimulation frequency and stimulation rate parameters to mask tinnitus; 2) Set the procedure of electric stimulation cochlear implant to mask tinnitus.

  • Research objectives 1) Summarize the changes of tinnitus after electrode implantation (effective treatment time, diseases suitable for electrical stimulation treatment, etc.); 2) Infer the mechanism of electric stimulation inhibiting tinnitus; 3) Set electrical stimulation parameters to effectively suppress tinnitus.
  • Scientific problems to be solved Our study group plan to use more advanced EEG technology to explore the principle of electric stimulation to suppress tinnitus, find out the effective scheme of electric stimulation to treat tinnitus, and help more patients solve the problem of tinnitus.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 1. This study included patients who received cochlear implants at the Auditory Implant Center of the Otorhinolaryngology-Head and Neck Surgery, China PLA General Hospital;
  • 2. The patients ranged from 16 to 90 years old;
  • 3. The patient experienced hearing loss and had either tinnitus longer than 0.25 years (experimental group 1) or no tinnitus (control group 2) before the cochlear implant surgery;
  • 4. The cochlear implants accepted by patients included products from MED-EL, Cochlear, Advanced Bionics and Nurotron;
  • 5. All patients voluntarily participated in the study.

Exclusion criteria

  • 1 Tinnitus types exclude non otogenic tinnitus (including tinnitus caused by hypertension, heart disease, hyperthyroidism, neurasthenia, hyperlipidemia, etc.);
  • 2 Contraindications of cochlear implant surgery (refer to the guidelines for cochlear implant 2013 of the Chinese Medical Association);
  • 3 Intellectual deficiency

Treatment and study plan

Cochlear Implant

Device

The surgeon will make a small cut (incision) behind patient's ear, and form a small hole in the portion of skull bone (mastoid) where the internal device rests. Then the surgeon create a small opening in the cochlea in order to thread the electrode of the internal cochlear implant device. The skin incision is stitched closed so that the internal device is under the skin.

Primary outcomes

  1. Electrical stimulation channel number

    Time frame: 1 week after operation

    Stimulating basement membrane with cochlear implant electrode to match tinnitus frequency. The cochlear implant electrode number is recorded.

  2. Electrical stimulation channel number

    Time frame: 1 month after operation

    frequency. The cochlear implant electrode number is recorded.

  3. Electrical stimulation channel number

    Time frame: 2 months after operation

    frequency. The cochlear implant electrode number is recorded.

  4. Electrical stimulation channel number

    Time frame: 3 months after CI operation

    frequency. The cochlear implant electrode number is recorded.

  5. Electrical stimulation channel number

    Time frame: 4 months after operation

    frequency. The cochlear implant electrode number is recorded.

  6. Electrical stimulation channel number

    Time frame: 7 months after operation

    frequency. The cochlear implant electrode number is recorded.

  7. Electrical stimulation channel number

    Time frame: 13 months after operation

    frequency. The cochlear implant electrode number is recorded.

  8. Electrical stimulation channel number

    Time frame: over 13 months after operation

    frequency. The cochlear implant electrode number is recorded.

  9. Tinnitus characteristic information questionnaire

    Time frame: Pre-operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  10. Tinnitus characteristic information questionnaire

    Time frame: 1 week after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  11. Tinnitus characteristic information questionnaire

    Time frame: 1 month after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  12. Tinnitus characteristic information questionnaire

    Time frame: 2 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  13. Tinnitus characteristic information questionnaire

    Time frame: 3 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  14. Tinnitus characteristic information questionnaire

    Time frame: 4 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  15. Tinnitus characteristic information questionnaire

    Time frame: 7 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  16. Tinnitus characteristic information questionnaire

    Time frame: 13 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  17. Tinnitus characteristic information questionnaire

    Time frame: over 13 months after operation

    A multifactorial and closed-ended questionnaire was developed by our CI center. The demographics and part of the tinnitus descriptions were recorded in Tinnitus Characteristics questionnaire for CI recipients. The patients' basic information, such as gender, age, aetiology, CI side, CI type, and time of deafness was completed by patients. Tinnitus characteristics information, including localization, duration, and type was collected for correlation analysis.

  18. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 1 week after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  19. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 1 month after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  20. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 2 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  21. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 3 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  22. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 4 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  23. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 7 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  24. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: 13 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  25. Tinnitus loudness(CI electrical stimulation intensity)

    Time frame: over 13 months after operation

    The tinnitus loudness was matched by the stimulation current level of cochlear implant electrode, The ultimate electrode stimulation current (IµA) is quantified in µA and the tinnitus loudness is recorded in Qtin (nC, 10-9C) (i.e. Qtin=IµA* tp).

  26. Objective electroencephalography-based assessment(EEG)

    Time frame: Pre-operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  27. Objective electroencephalography-based assessment(EEG)

    Time frame: 1 week after operation

    The EEG waveforms of CI patients were tested, and the amplitude and latency were recorded.

  28. Objective electroencephalography-based assessment(EEG)

    Time frame: 1 month after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  29. Objective electroencephalography-based assessment(EEG)

    Time frame: 2 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  30. Objective electroencephalography-based assessment(EEG)

    Time frame: 3 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  31. Objective electroencephalography-based assessment(EEG)

    Time frame: 4 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  32. Objective electroencephalography-based assessment(EEG)

    Time frame: 7 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  33. Objective electroencephalography-based assessment(EEG)

    Time frame: 13 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  34. Objective electroencephalography-based assessment(EEG)

    Time frame: over 13 months after operation

    EEG is a non-invasive objective assessment technique that records brain activity along with specific neural pathways. we utilize cortical auditory evoked potential (CAEP) and event-related potentials(ERP) to obtain time-domain analysis.

  35. Speech perception

    Time frame: Pre-operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  36. Speech perception

    Time frame: 1 months after operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  37. Speech perception

    Time frame: 2 month after operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  38. Speech perception

    Time frame: 4 months after operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  39. Speech perception

    Time frame: 7 months after operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  40. Speech perception

    Time frame: 13 months after CI operation

    The patient are tested for speech recognition and the results were recorded as a percentage

  41. Speech perception

    Time frame: over 13 months after CI activation

    The patient are tested for speech recognition and the results were recorded as a percentage

Secondary outcomes

  1. Pure tone test

    Time frame: pre-operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  2. Pure tone test

    Time frame: 1 month after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  3. Pure tone test

    Time frame: 2 months after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  4. Pure tone test

    Time frame: 4 months after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  5. Pure tone test

    Time frame: 7 month after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  6. Pure tone test

    Time frame: 13 month after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  7. Pure tone test

    Time frame: over 13 month after operation

    Evaluation of 250-8000hz hearing effect in patients with hearing loss

  8. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: Pre-operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  9. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: 1 month after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  10. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: 2 months after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  11. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: 4 months after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  12. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: 7 months after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  13. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: 13 months after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

  14. Self-Rating Anxiety Scale (SAS) questionnaire

    Time frame: over 13 months after operation

    Assessment of patients' mental state （depression, anxiety, insomnia），The result analysis chart of this system shows the standard score. The higher the score, the more serious the symptoms in this regard. Generally speaking, those whose total anxiety score is less than 50 are normal; 50-60 is mild, 61-70 is moderate, and more than 70 is severe anxiety. The number of negative items means the number of items on which the subject did not respond, and the number of positive items means the number of items on which the subject responded. Total rough score: the scores of 20 items are added together, and the demarcation score is 40 points.

Study contacts

Contact information is provided by the study sponsor or research team.

QIAN WANG, M.S.

CONTACT

[email protected]

+8618211068103

Shi m Yang

CONTACT

[email protected]

01068159050

Sponsors and collaborators

Lead sponsor

Chinese PLA General Hospital

Other

Registry information

Official study title

Effects of Cochlear Implantation on Tinnitus and Its Symptoms

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Jul 12, 2022
Registry last updated
Jun 6, 2023

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