Factors Associated With Quality of Dreams During General Anesthesia

December 17, 2021 updated by: Bijia Song, Beijing Friendship Hospital

Factors Associated With Quality of Dreams During General Anesthesia: a Prospective Observational Study

Patients frequently report having dreams during general anesthesia. The incidence of dreams during general anesthesia that have been reported by patients upon awakening has been reported to range from 10 to 36% [1] and to be higher in younger patients, female patients [2], and patients who received ketamine [3]. The quality of dreams during general anesthesia is often reported as pleasant, but some patients report unpleasant or not pleasant dreams [4, 5]. However, the factors associated with the quality of dreams have remained to be elucidated. Therefore, the aim of this study was to determine the relationships between the quality of dreams during general anesthesia and perioperative factors.

Study Overview

Status

Not yet recruiting

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

200

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

We recruited patients who were more than 20 years of age and who were scheduled for elective surgery under general anesthesia regardless of the type of surgery

Description

Inclusion Criteria:

  • We recruited patients who were more than 20 years of age
  • Patients who were scheduled for elective surgery under general anesthesia regardless of the type of surgery

Exclusion Criteria:

  • diagnosis of a psychological disorder,
  • major afective disorder
  • major drug dependence disorder,
  • inability to understand the content of our study,
  • planned postoperative ventilation,
  • anticipation of unavailability for postoperative interviews

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
General anesthesia Group

Patients frequently report having dreams during general anesthesia, and the dreams are often reported to be pleasant dreams.

However, factors associated with the quality of dreams during general anesthesia have not been clarifed. The aim of this study was to determine the relationships between the quality of dreams during general anesthesia and perioperative factors.

This prospective observational study included patients scheduled for elective surgery under general anesthesia.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anesthesia information
Time Frame: During the operation
Anesthesia was maintained with a general anesthetic (propofol, sevofurane, or desfurane) and remifentanil. Some patients also received a peripheral nerve block. Anesthetic management including the choice of a general anesthestic (propofol, sevofurane, or desflurane) depended on the decision of the anesthesiologists in charge
During the operation
Dream interview
Time Frame: After extubation, patients were interviewed about intraoperative dreams in the operating room as soon as they were oriented to time, place, and person

The following questions were asked.

  1. What was the last thing you remember before going to sleep?
  2. What was the frst thing you remember from when you woke up?
  3. Can you recall anything between?
  4. Did you have any dreams while under anesthesia?
  5. How did you feel about your dream: pleasant, indiferent or unpleasant?
After extubation, patients were interviewed about intraoperative dreams in the operating room as soon as they were oriented to time, place, and person
Depression level
Time Frame: the day before surgery
The Hospital Anxiety and Depression Scale (HADS), which is a self-report questionnaire, was used for evaluation of anxious and depressive states in the participants
the day before surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

January 1, 2022

Primary Completion (Anticipated)

June 30, 2022

Study Completion (Anticipated)

June 30, 2022

Study Registration Dates

First Submitted

December 17, 2021

First Submitted That Met QC Criteria

December 17, 2021

First Posted (Actual)

January 5, 2022

Study Record Updates

Last Update Posted (Actual)

January 5, 2022

Last Update Submitted That Met QC Criteria

December 17, 2021

Last Verified

December 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • General anesthesia and dream

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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