Status:
ACTIVE_NOT_RECRUITING
Effect of Discontinuing Propofol After Cecal Intubation on Patient's Psychomotor Recovery Following Colonoscopy
Lead Sponsor:
American University of Beirut Medical Center
Conditions:
Procedural Sedation
Colonoscopy
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
This study investigates whether discontinuing the continuous intravenous infusion of propofol immediately after cecal intubation would reduce the patient's recovery time without compromising their com...
Detailed Description
Colonoscopy is usually conducted after inducing depression in the patient's level of consciousness through sedation, ranging from minimal anxiolysis to general anesthesia, to establish relief from pot...
Eligibility Criteria
Inclusion
- Age between 18 and 80 years.
- Scheduled ambulatory elective screening or surveillance colonoscopy under MAC.
Exclusion
- Medical contraindication to anesthesia (i.e., respiratory/cardiac/neurologic compromise, known allergy or adverse reaction to propofol, midazolam, lidocaine, or opiates, …)
- History of ischemic or hemorrhagic cerebrovascular accident.
- Baseline cognitive dysfunction (impaired memory, attention deficit, language disorders, …) - in other words, any dysfunction that prevents the subject from understanding the study protocol and/or completing the requested tests and assessments (e.g., playing the minigames, …)
- Use of more than one psychoactive drug.
- History of partial colectomy.
- Unable to give consent.
Key Trial Info
Start Date :
May 19 2025
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2025
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT07168135
Start Date
May 19 2025
End Date
December 1 2025
Last Update
September 11 2025
Active Locations (1)
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1
The American University of Beirut Medical Center
Beirut, Lebanon, 1107