Insufflation with CO2 versus room air in colonoscopy
Phase 2
- Conditions
- Patients indicated for Colonoscopy
- Registration Number
- RPCEC00000186
- Lead Sponsor
- ational Centre for Minimal Access Surgery (CNCMA)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Male and female patients with 18 or more years old
Exclusion Criteria
1. Severe respiratory illness (hospitalization in the last 6 months or home oxygen therapy),
2. Sleep Apnea.
3. Morbid obesity. (BMI = 35)
4. Inability to understand the study.
5. Performing on the day of upper endoscopy and colonoscopy.
6. Making sigmoidoscopy
7. Patients who refuse consent for participation in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain (Visual Analogue Scale). Measuring time: 15 minutes, 1 hour after procedure.
- Secondary Outcome Measures
Name Time Method umber of Propofol ( Total amount of anesthetic was required) Measuring time: After procedure.<br>Total Time (Time elapsed since the start of colonoscopy until completion the procedure) Measuring time: After procedure.<br>CO2 pressure ( Value of measuring CO2 in the patient ) Measuring time: before, during and after procedure.<br>O2 Saturation( Value of measuring O2 presented by the patient) Measuring time: before, during and after procedure.<br>Heart rate (number of heartbeats in the patient) Measuring time: before, during and pafter procedure.<br>Complications (Presence of complications due to come) Measuring time: during and after procedure.