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Clinical Trial Summary

The purpose of this study is to compare a new method: the combination of conscious sedation with remifentanil (a shortlasting opioid drug) and local anaesthesia, with the traditional general anaesthesia for hysteroscopic surgery. The primary outcomes are: the time spent in the operation room, the time to full mobilisation postoperatively and the time to complete recovery postoperatively and the time to discharge. Secondary outcome: patient satisfaction.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT00763789
Study type Interventional
Source Copenhagen University Hospital at Herlev
Contact Birgitte Majholm, MD
Phone +4544883595
Email Birmaj01@heh.regionh.dk
Status Recruiting
Phase N/A
Start date August 2008
Completion date September 2010

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