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NCT Number: NCT06170021

Occurrence of Radiation-induced Otitis Media in Nasopharyngeal Carcinoma Patients After Intensity Modulated Radiotherapy

This is an observational cohort study to investigate the incidence of radiation-induced otitis media, changes in tubal function and hearing in newly diagnosed nasopharyngeal carcinoma patients without metastasis at multiple time points from baseline to 1 year after radiotherapy.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, 510060, China

Location status: Recruiting

Location contact

Haiqiang Mai, MD,Ph.D

CONTACT

[email protected]

86-20-8734-3643

About this study

Patients with newly diagnosed non-metastatic nasopharyngeal carcinoma (AJCC 8th) will be recruited. The incidence of radiation-induced otitis media, eustachian tube function and hearing level in nasopharyngeal carcinoma patients will be prospectively evaluated by magnetic resonance imaging, otoscope, pure tone audiometry, acoustic immittance test and the Eustachian Tube Dysfunction Questionnaire (ETDQ-7) before treatment and serially up to 1 year after radiotherapy. The quality of life of patients will be evaluated before treatment and serially up to 1 year after radiotherapy. The incidence of radiation-induced otitis media, the changes of eustachian tube function and hearing level, together with the influencing factors, in nasopharyngeal carcinoma patients after induction chemotherapy and concurrent chemoradiotherapy will be investigated.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18-70, regardless of sex.
  • ECOG (Eastern Cooperative Oncology Group) score: 0-1.
  • Patients must sign informed consent and be willing, and well understood the objective and procedure of this study.
  • Patients with newly histologically confirmed non-keratinizing nasopharyngeal carcinoma, type of WHO II or III, clinical stage I-IVa (according to the 8th American Joint Committee on Cancer [AJCC] edition.
  • No radiotherapy or chemotherapy was administered before enrollment.
  • Expected survival time ≥ 6 months.

Exclusion criteria

  • Women in pregnancy or lactation.
  • Patients with significantly lower heart, liver, lung, kidney, bone marrow function and other severe medical condition.
  • Prior to radiotherapy, there is a clear underlying disease of the eustachian tube or other ear diseases.
  • Patients with otitis media before radiotherapy and have no improvement at the end of radiotherapy.
  • Patients with history of middle ear, nasal or nasopharyngeal surgery on the affected side.
  • Patients combined with congenital cleft palate and other craniofacial abnormalities.
  • Patients with histologically confirmed keratinizing nasopharyngeal carcinoma, type of WHO I.
  • Patients with recurrence and distant metastasis.
  • Patients with radiotherapy or chemotherapy before.
  • Age < 18 or age > 70.
  • Patients who changed their initial treatment regimen during the observation period due to disease progression (including tumor residual after radiotherapy, tumor recurrence, and new distant metastases).

Treatment and study plan

Primary outcomes

  1. Incidence of radiation-induced otitis media

    Time frame: 1 year

    Incidence of radiation-induced otitis media will be assessed prospectively before treatment and serially up to 1 year after radiotherapy by magnetic resonance imaging, otoscope, acoustic immittance test and pure tone audiometry.

Secondary outcomes

  1. Effect of the irradiation dose of eustachian tube, tympanum, cochlea, internal auditory tract and vestibule on the occurrence of radiation-induced otitis media

    Time frame: 1 year

    The occurrence of radiation-induced otitis media will be assessed prospectively before treatment and serially up to 1 year after radiotherapy by magnetic resonance imaging, otoscope, acoustic immittance test and pure tone audiometry.

  2. Effect of irradiation dose in the area around of eustachian tube on the severity of ototoxicity after radiotherapy

    Time frame: 1 year

    Severity of ototoxictiy will be assessed prospectively before treatment and serially up to 1 year after radiotherapy by magnetic resonance imaging, otoscope, acoustic immittance test, pure tone audiometry and the Eustachian Tube Dysfunction Questionnaire (ETDQ-7).

  3. Effect of irradiation dose of eustachian tube on hearing injury

    Time frame: 1 year

    The injury of hearing will be assessed prospectively before treatment and serially up to 1 year after radiotherapy by acoustic immittance test and pure tone audiometry.

  4. Effect of different chemoradiotherapy treatment regimens on the occurrence of radiation-induced otitis media

    Time frame: 1 year

    The occurrence of radiation-induced otitis media will be assessed prospectively before treatment and serially up to 1 year after radiotherapy by magnetic resonance imaging, otoscope, acoustic immittance test and pure tone audiometry.

  5. Correlation between radiation-induced otitis media and life quality after radiotherapy

    Time frame: 1 year

    The life quality will be assessed prospectively before treatment and serially up to 1 year after radiotherapy.

Study contacts

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

Haiqiang Mai, Dr

CONTACT

[email protected]

86-20-8734-3643

Qiuyan Chen, Dr

CONTACT

[email protected]

86-20-8734-3380

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Official study title

Effect of Irradiation Dose to Eustachian Tube and Surrounding Auditory Organs on the Occurrence of Radiation-induced Otitis Media in Nasopharyngeal Carcinoma Patients During Intensity Modulated Radiotherapy Era: A Prospective Cohort Study

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Dec 14, 2023
Registry last updated
Aug 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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