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NCT Number: NCT05173688

The Relationship Between Different Doses of Propofol and the Occurrence of Dreams in Short Surgery Under General Anesthesia

Dreams are a remarkable experiment in psychology and neuroscience, conducted every night in every sleeping person. 74% of awakenings from REM sleep resulted in recall of a dream, as compared with only 9% of awakenings from NREM sleep. The association between dreaming and REM sleep was subsequently replicated by many other investigators; typically, around 80% of REM awakenings yield dreams. It became clear over time that there is a good deal of mental activity that occurs during NREM sleep. Typically, it is more thought like, fragmentary, and related to daily concerns than the vivid, hallucinatory, predominantly visual narratives that are most commonly reported from REM sleep. But even this distinction appears not to be absolute. There is now wide acceptance of the view that some dreaming that is indistinguishable from REM sleep dreaming occurs in NREM sleep, most frequently in the sleep-onset period. General anesthesia causes a drug-induced state of unconsciousness and is a non-physiological process that is similar to natural sleep. Patients receiving propofol for maintenance of general anesthesia often report higher incidences of dreaming than patients maintained with volatile anesthetics. One explanation is that propofol and volatile anesthetic have different pharmacological effects in the central nervous system. An alternative explanation is that propofol is associated with more rapid emergence from anesthesia than the older volatile anesthetics, allowing patients to report their dreams before they are forgotten. In order to further verify the hypothesis, the investigators choose gynecological general anesthesia to observe whether the generation of dreams is related to the dose of general anesthesia maintenance .

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Key information

Age range

18 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Shengjing Hospital

Shenyang, Liaoning, 110004, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • between 18 and 70 years
  • with an ASA physical status of I or II

Exclusion criteria

  • presence of sleep disorders
  • pain syndrome
  • cardiovascular disease
  • sleep apnea syndrome
  • psychosis
  • history of opioid usage
  • history of abnormal operation or anesthesia recovery
  • unwillingness to provide informed consent
  • a patient with a language communication disorder

Treatment and study plan

Propofol

Drug

The low maintenance dose propofol group was maintained at 4-6 mg/kg/h ;and The high maintenance dose propofol group was maintained at 8-12 mg/kg/h

Primary outcomes

  1. Mean blood pressure (systolic and diastolic)

    Time frame: 5 minutes after entering the operation room

    record mean blood pressure during the surgery

  2. Mean blood pressure (systolic and diastolic)

    Time frame: Anesthesia induction to fall asleep

    record mean blood pressure during the surgery

  3. Mean blood pressure (systolic and diastolic)

    Time frame: at the end of surgery

    record mean blood pressure during the surgery

  4. Mean blood pressure (systolic and diastolic)

    Time frame: Upon awakening from anesthesia

    record mean blood pressure during the surgery

  5. Mean blood pressure (systolic and diastolic)

    Time frame: leaving the operation room

    record mean blood pressure during the surgery

  6. heart rate

    Time frame: entering the operation room

    record heart rate during the surgery

  7. heart rate

    Time frame: Anesthesia induction to fall asleep

    record heart rate during the surgery

  8. heart rate

    Time frame: at the end of surgery

    record heart rate during the surgery

  9. heart rate

    Time frame: Upon awakening from anesthesia

    record heart rate during the surgery

  10. heart rate

    Time frame: leaving the operation room

    record heart rate during the surgery

  11. BIS

    Time frame: entering the operation room

    record BIS during the surgery

  12. BIS

    Time frame: Anesthesia induction to fall asleep

    record BIS during the surgery

  13. BIS

    Time frame: at the end of surgery

    record BIS during the surgery

  14. BIS

    Time frame: Upon awakening from anesthesia

    record BIS during the surgery

  15. BIS

    Time frame: leaving the operation room

    record BIS during the surgery

  16. Total dose of propofol

    Time frame: at the end of surgery

    record total dose of propofol

  17. Dream

    Time frame: at the end of surgery

    Dreaming during anesthesia was defined as any experience that was described by the patient as dreaming and was thought by the patient to have occurred between the induction of anesthesia and the first moment of consciousness after anesthesia.27 Awareness was defined as postoperative recall of intraoperative events. All patients who reported dreaming were considered to be "dreamers" for the purpose of the analyses, whether or not they could remember the narrative of the dream. However, only dreaming reports where the narrative was remembered were classified using five-point Likert scales as follows. Emotional content (1 very negative; 5 very positive) ● Memorability (1 can't remember narrative of dream; 5 most memorable ever) ● Visual vividness (1 not at all vivid; 5 most vivid ever) ● Amount of sound (1 no sound; 5 most sound ever)

Secondary outcomes

  1. Postoperative adverse effects

    Time frame: 24 hours after surgery

    record postoperative adverse effects

Sponsors and collaborators

Lead sponsor

Shengjing Hospital

Other

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Dec 30, 2021
Registry last updated
Jun 2, 2022

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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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