Trials / Terminated
TerminatedNCT01362075
Pain Management After Shoulder Prosthesis: A Clinical Trial of Nerve Block and Local Infiltration
Pain Management After Shoulder Arthroplasty: A Randomised Clinical Trial of Interscalene Block and Local Infiltration Analgesia
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 74 (actual)
- Sponsor
- Horsens Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the efficacy of local infiltration analgesia as compared to 48-hour interscalene block in treating pain after shoulder arthroplasty. The investigators hypothesize a reduced pain score and use of supplemental analgesic medication during the first three postoperative days using local infiltration analgesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Local infiltration analgesia | 150 ml ropivacaine, of which 100 ml is with adrenalin |
| PROCEDURE | Interscalene catheter | 7 ml ropivacaine interscalene block via catheter, subsequently given 5 ml/h and possibility of 5 ml bolus for the first 48 hours. |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2014-07-01
- Completion
- 2014-10-01
- First posted
- 2011-05-27
- Last updated
- 2014-08-08
Locations
2 sites across 1 country: Denmark
Source: ClinicalTrials.gov record NCT01362075. Inclusion in this directory is not an endorsement.