- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05813262
Patient Opinions Regarding General Anesthesia, Before and After Having Undergone a Procedure.
April 2, 2023 updated by: Dr. Gordon MacGregor, Alabama College of Osteopathic Medicine
The goal of this survey will be to assess the opinions and reticence of patients who have undergone surgical procedures that required the usage of general anesthesia both before they underwent the procedure and afterwards.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
217
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Alabama
-
Ashford, Alabama, United States, 36312
- Ashford Clinic
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
Participants will be recruited from physicians offices in Alabama and Florida.
Recruitment will be via posters displayed at one of these three locations.
Participants will also be recruited via social media platforms.
Description
Inclusion Criteria:
- Have experience with general anesthesia.
Exclusion Criteria:
- Anyone who has not undergone a procedure using general anesthesia and who will not undergo such a procedure within the next 6 months.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived level of anxiety towards general anesthesia
Time Frame: From exposure to general anesthesia until survey completion by September 2022
|
The perceived level of anxiety (on a scale of 1 to 10) before and after undergoing general anesthesia
|
From exposure to general anesthesia until survey completion by September 2022
|
|
Perceived level of danger towards general anesthesia
Time Frame: From exposure to general anesthesia until survey completion by September 2022
|
The perceived level of danger (on a scale of 1 to 10) before and after undergoing general anesthesia
|
From exposure to general anesthesia until survey completion by September 2022
|
|
Perceived side effects of general anesthesia
Time Frame: From exposure to general anesthesia until survey completion by September 2022
|
Description of perceived side effects
|
From exposure to general anesthesia until survey completion by September 2022
|
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 (Actual)
May 3, 2022
Primary Completion (Actual)
July 8, 2022
Study Completion (Actual)
September 23, 2022
Study Registration Dates
First Submitted
April 2, 2023
First Submitted That Met QC Criteria
April 2, 2023
First Posted (Actual)
April 14, 2023
Study Record Updates
Last Update Posted (Actual)
April 14, 2023
Last Update Submitted That Met QC Criteria
April 2, 2023
Last Verified
April 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- HS220404
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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