Trials / Completed
CompletedNCT01025102
The Addition of Sufentanil Interscalene Block in Shoulder Surgery
Phase III Study of the Addition of Sufentanil to Interscalene Block in Shoulder Surgery
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Bent Gymoese Jorgensen · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the effects and side effects of interscale block performed with Naropin 0.1% cum sufentanil or Naropin 0.1% in shoulder surgery.
Detailed description
The purpose of this study is to compare the duration of postoperative analgesia and supplemental opioid consumption and side effects of interscale block performed with Naropin 0.1% cum sufentanil or Naropin 0.1% in shoulder surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Naropin 0.1% cum sufentanil | 20ml of Naropin 0.1% cum sufentanil 1mikrog per ml |
Timeline
- Start date
- 2010-01-01
- Primary completion
- 2012-11-01
- Completion
- 2012-12-01
- First posted
- 2009-12-03
- Last updated
- 2013-04-02
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01025102. Inclusion in this directory is not an endorsement.