Clinical Trials Directory

Trials / Completed

CompletedNCT01377415

Continuous Subacromial Bupivacaine

The Analgesic Effect of Continuous Subacromial Bupivacaine Infusion After Arthroscopic Shoulder Surgery: a Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Turku University Hospital · Other Government
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The investigators wanted to re-evaluate the effects of subacromial bupivacaine infusion after shoulder arthroscopy with standard surgical techniques, including rotator cuff operations. The investigators hypothesized that patients having 5.0 mg/ml bupivacaine infusion at a rate of 2 ml/h subacromially would need less opioids than patients receiving a placebo infusion.

Detailed description

Shoulder surgery has become a routine outpatient procedure. Previously shoulder surgery was associated with intense, occasionally severe postoperative pain and hence considerable use of opioids. Also arthroscopic shoulder surgery, especially rotator cuff procedures, may cause significant pain resulting sometimes in inpatient admission. Subacromial local anaesthetic infusion as a part of a multimodal approach is one commonly used modality to pain relief after shoulder surgery. Nevertheless, it has been criticized recently for its poor benefits and possible adverse effects. On the whole, the scientific evidence of the advantages of local anaesthetic infusions is inconclusive.

Conditions

Interventions

TypeNameDescription
DRUGbupivacainebupivacaine 5 mg/ml infusion 2 ml/h 48 h

Timeline

Start date
2009-01-01
Primary completion
2010-06-01
Completion
2010-06-01
First posted
2011-06-21
Last updated
2011-06-22

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01377415. Inclusion in this directory is not an endorsement.