A clinical study comparing two regimens of bowel preparation for colonoscopy
Phase 4
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2018/10/015926
- Lead Sponsor
- JIPMER intramural research fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Consecutive consenting patients of both gender aged 18 years and above posted for elective colonoscopy in the department of Medical Gastroenterology, JIPMER
Exclusion Criteria
a.Presence of severe renal impairment (creatinine clearance less than 30 mL per min)
b.Patients on hemodialysis
c.Pregnant or lactating women
d.Severe congestive heart failure (NYHA 3 or 4)
e.History of bowel obstruction or resection
f.Known allergies to polyethylene glycol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the efficacy of same day polyethylene glycol preparation with 10 mg bisacodyl as compared with low volume split dose polyethylene glycol preparation with 10mg bisacodyl on the adequacy of bowel preparation in patients undergoing colonoscopy based on Boston bowel preparation score.Timepoint: During the procedure (colonoscopy)
- Secondary Outcome Measures
Name Time Method To compare the patient tolerability, acceptability and compliance between the two groups using validated questionnaires.Timepoint: Before the procedure (colonoscopy)