Additive Effects of Clonidine Used in Propofol Sedation in Colonoscopy
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorTanta University
About this trial
The objective of this study was to compare safety, satisfaction, and efficiency outcomes of propofol versus propofol with clonidine in patients undergoing colonoscopy.
Eligibility criteria
Qualifiers
Age 18-65 years.
Both sexes.
American Society of Anesthesiology (ASA) physical status I-II.
Patients undergoing colonoscopy.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Propofol
- Propofol combined with clonidine
Treatment groups
62 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov