Actively Recruiting
Comparison of Safety and Efficacy for Different Sedation Regimens During Colonoscopy
Led by Qassim Health Cluster · Updated on 2025-07-25
157
Participants Needed
1
Research Sites
28 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a randomized, double-blinded, prospective study which will be conducted at the Department of Gastroenterology, King Saud Hospital, Unaizah, Qassim, Saudi Arabia. This study aims to compare safety and efficacy of different types of sedation medications for elective colonoscopy. Colonoscopy is a procedure to examine and visualize the colon by a fiberoptic tube called colonoscope. Sedation helps one to relax to avoid feel any discomfort or pain during the procedure.
CONDITIONS
Official Title
Comparison of Safety and Efficacy for Different Sedation Regimens During Colonoscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18-60 years
- Both genders
- Scheduled for colonoscopy without advanced intervention
- ASA physical status I or II
- Able to give informed consent
You will not qualify if you...
- Allergic reaction or contraindication to midazolam, propofol, or fentanyl
- Age below 18 or above 60 years
- Chronic benzodiazepine use
- ASA physical status III or higher
- Pregnancy
- History of smoking or alcohol abuse
- Body mass index greater than 35 kg/m2
- History of airway obstruction or difficult intubation
AI-Screening
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Trial Site Locations
Total: 1 location
1
King Saud Hospital
Unaizah, Al-Qassim Region, Saudi Arabia, 56437
Actively Recruiting
Research Team
M
Mohammed S Alsulaimi, consultant gastroenterologist
CONTACT
M
Muhammad Y Memon, FCPS,MRCP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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