- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05179590
Factors Associated With Quality of Dreams During General Anesthesia
Factors Associated With Quality of Dreams During General Anesthesia: a Prospective Observational Study
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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.
|
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
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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