Clinical Trials Directory

Trials / Completed

CompletedNCT01550952

Interscalene Dynamometer Pilot Study

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
Hospital for Special Surgery, New York · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Total shoulder arthroplasty (shoulder replacement) can cause severe postoperative pain. Commonly, patients receive general anesthesia with interscalene block (injection of local anesthetic or numbing medicine near nerves in the shoulder) during surgery. As a result of the interscalene block, patients often experience sensory and motor blockade. The purpose of this study is to determine the effects of the interscalene block on the anterior deltoid muscle and hand grip strength after total shoulder arthroplasty.

Detailed description

Total shoulder arthroplasty can cause severe postoperative pain. Pain management includes general anesthesia with interscalene block during surgery and intravenous (IV) hydromorphone patient controlled analgesia (PCA) and oral opioid analgesics given after surgery. Side effects, such as motor blockade, may impair participation in physical therapy and diminish patient satisfaction. In order to prepare for a future study that will examine what mixtures of adjuncts/additives will best prevent recovery room pain and minimize motor blockade, the investigators are conducting this pilot study to collect preliminary data on current practice. The investigators believe the current regimen will provide adequate pain relief, but may cause extensive motor blockade and reduce patients' muscle strength after surgery.

Conditions

Timeline

Start date
2011-12-01
Primary completion
2012-02-01
Completion
2012-02-01
First posted
2012-03-12
Last updated
2016-03-31
Results posted
2016-03-31

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01550952. Inclusion in this directory is not an endorsement.