Status:
RECRUITING
Additive Effects of Clonidine Used in Propofol Sedation in Colonoscopy
Lead Sponsor:
Tanta University
Conditions:
Clonidine
Propofol
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
The objective of this study was to compare safety, satisfaction, and efficiency outcomes of propofol versus propofol with clonidine in patients undergoing colonoscopy.
Detailed Description
Colonoscopy is one of the most common procedures in the world, Colonoscopy is a procedure often performed for prevention, diagnosis, and treatment of a variety of symptoms and diseases of the lower di...
Eligibility Criteria
Inclusion
- Age 18-65 years.
- Both sexes.
- American Society of Anesthesiology (ASA) physical status I-II.
- Patients undergoing colonoscopy.
Exclusion
- Patients had recent history of colonoscopy.
- Previous colonic resection.
- Severe heart failure (ejection fraction \< 30%).
- Known history of hypersensitivity to propofol or clonidine and any need for anesthetic drug administration other than the study protocol.
Key Trial Info
Start Date :
July 20 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2024
Estimated Enrollment :
62 Patients enrolled
Trial Details
Trial ID
NCT06507410
Start Date
July 20 2024
End Date
September 1 2024
Last Update
July 23 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Tanta University
Tanta, El-Gharbia, Egypt, 31527