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Capnographic Monitoring of Propofol-sedation During Colonoscopy

Hypoxia Clinical Trial

Official title:
Capnographic Monitoring of Propofol-sedation During Colonoscopy

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01638793
Study type Interventional
Source Johann Wolfgang Goethe University Hospitals
Contact
Status Completed
Phase N/A
Start date June 2012
Completion date September 2013
View Details
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