Trials / Completed
CompletedNCT01638793
Capnographic Monitoring of Propofol-sedation During Colonoscopy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 528 (estimated)
- Sponsor
- Johann Wolfgang Goethe University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The present study is a randomized, prospective, single-blinded study. Patients presenting for colonoscopy under sedation will be included according to the statistical sample size calculation. Patients will be randomized to either group 1- capnographic monitoring or group 2- oxygenic monitoring during Propofol-based sedation for colonoscopy. Episodes of Hypoxia are documented and compared in both groups.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Microcap (Oridion, Needham, MA, USA) | |
| DEVICE | Smart Capno Line Plus O2 (Oridion, Needham, MA, USA) |
Timeline
- Start date
- 2012-06-01
- Primary completion
- 2013-09-01
- Completion
- 2013-09-01
- First posted
- 2012-07-12
- Last updated
- 2013-10-25
Locations
2 sites across 1 country: Germany
Source: ClinicalTrials.gov record NCT01638793. Inclusion in this directory is not an endorsement.