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
| Type | Name | Description |
|---|---|---|
| DRUG | Sedation 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.