Trial Details
Not RecruitingBasic Information
| Clinical ID | c5105 |
|---|---|
| Identifier | EUCTR2013-002428-17-DK |
| Trial Title | Nurse Administered Propofol Sedation vs combined sedation with midazolam/fentanil for colonoscopy in patients with IBD. A randomised controlled trial of satisfaction and adhearence to treatment program. - Propofol vs. standard sedation for colonoscopy. A |
| Trial URL | Visit Original Page |
Study Information
| Study Results | NULL |
|---|---|
| Conditions | Satisfaction with sedation during colonoscopy in patients with inflammatory bowel disease MedDRA version: 14.1.Level: LLT.Classification code 10049683.Term: Monitored anesthesia care sedation.System Organ Class: 1000000 |
| Interventions | Trade Name: Propofol B. BraunProduct Name: Propofol B. BraunPharmaceutical Form: Emulsion for infusionINN or Proposed INN: PropofolCAS Number: 2078-54-8Other descriptive name: PROPOFOLConcentration unit: mg/ml milligram(s)/ |
Participant Information
| Sponsor | Gastroenheden D, Herlev Hospital |
|---|---|
| City | NULL |
| Country/Region | Denmark |
Enrollment Criteria
| Sex Requirement | NOT SPECIFIED |
|---|---|
| Age Requirement | NULL |
Study Design
| Study Type | Interventional clinical trial of medicinal product |
|---|---|
| Phase | NULL |
Time Information
| Start Date | NULL |
|---|---|
| Primary Completion Date | NULL |
| Completion Date | NULL |