Clinical Trials Directory

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

TypeNameDescription
DRUGNaropin 0.1% cum sufentanil20ml 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.