Additive Effects of Clonidine Used in Propofol Sedation in Colonoscopy
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The objective of this study was to compare safety, satisfaction, and efficiency outcomes of propofol versus propofol with clonidine in patients undergoing colonoscopy.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:
• Age 18-65 years.
• Both sexes.
• American Society of Anesthesiology (ASA) physical status I-II.
• Patients undergoing colonoscopy.
Locations
Other Locations
Egypt
Tanta University
RECRUITING
Tanta
Contact Information
Primary
Rabab M Mohamed, MD
rabmoh_30@outlook.com
00201069122935
Time Frame
Start Date: 2024-07-20
Estimated Completion Date: 2024-09-01
Participants
Target number of participants: 62
Treatments
Active_comparator: Propofol group
Patients will receive induction of sedation as follow:~Continuous propofol infusion will be given with syringe pump for maintenance, with the initial rate set at 25-75 mic/kg/min IV during the first 10-15 min. To avoid administering sedatives at rates greater than clinically necessary, infusion rates will be gradually titrated to 25-50 mic/kg/min and regulated with the clinical response, with an onset of peak drug action expected to occur within 2 min.
Experimental: Propofol combined with clonidine group
Patients will receive 2 μg/kg of clonidine for injection intravenously 30 min before induction of sedation, administered over 10 min.
Related Therapeutic Areas
Sponsors
Leads: Tanta University