EUCTR2004-002966-39-GBActive, not recruitingNot Applicable
A Double-blind randomised controlled trial to compare buscopan versus placebo as an adjunct to colonoscopy
Sheffield Teaching Hospitals NHS Foundation Trust0 sites300 target enrollmentStarted: January 8, 2007Last updated:
Conditions
Drugs
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Enrollment
- 300
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •all patients due to undergo colonoscopy at the Northern General Hospital in Sheffield will be invited to take part in this study. This will include patients requesting Midazolam (intravenous sedation) or Entonox (inhaled analgesia) during their colonoscopy.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •allergy to buscopan; previous bowel resection; glaucoma; obstructive uropathy; autonomic dysfunction; myasthenia gravis; concurrent anticholinergic medication;l inability to consent or understand or read English.
Investigators
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