Clinical Trials Directory

Trials / Terminated

TerminatedNCT00326352

Comparison of Sedation/Analgesia: Midazolam/Morphine Vs Propofol/Remifentanil

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
40 (planned)
Sponsor
University of Edinburgh · Academic / Other
Sex
All
Age
16 Years – 65 Years
Healthy volunteers
Not accepted

Summary

For reduction of dislocated shoulder, sedation with propofol and remifentanil should give satisfactory operating conditions and pain relief, and significantly reduce the time to full recovery, compared with morphine and midazolam

Detailed description

Propofol is a recognised agent for sedation and remifentanil is a short acting opioid analgesic. We intend to provide sedation with propofol, 0.5 mg/Kg, and analgesia with remifentanil 0.5 microgram/Kg for reduction of dislocated shoulders. This will be a randomised sex-stratified comparison with current therapy which is midazolam incrementally up to a maximum of 0.15 mg/Kg, and morphine incrementally up to 0.15 mg/Kg. The primary outcome measure is time to full recovery. Secondary aspects are pain or discomfort during the procedure and operating conditions.

Conditions

Interventions

TypeNameDescription
DRUGSedation with propofol and remifentanil

Timeline

Start date
2003-07-01
Completion
2005-06-01
First posted
2006-05-16
Last updated
2006-05-16

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00326352. Inclusion in this directory is not an endorsement.