Interscalene Dynamometer Pilot Study
Completed
Conditions studied: Total Shoulder Arthroplasty
In brief
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.
Key facts
- Study ID
- NCT01550952
- Run by
- Hospital for Special Surgery, New York
- People needed
- 10
- Starts
- 2011-12-01
- Expected to finish
- 2012-02-01
- Last updated by the study team
- 2016-03-31
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients scheduled for primary total shoulder arthroplasty
- Age 18 to 80 years old
- Planned use of general anesthesia via laryngeal mask airway (LMA) and peripheral nerve block
- Ability to follow study protocol
- Patients with American Society of Anesthesiologists (ASA) physical status of I, II or III
You may not qualify if…
- Patients younger than 18 years old and older than 80
- Patients not intending to receive general anesthesia and peripheral nerve block
- Allergy or intolerance to one of the study medications
- Patients with an ASA of IV
- Hepatic or renal insufficiency
- Chronic opioid use (taking opioids for longer than 3 months)
Where it is running
- Hospital for Special Surgery — New York, New York, United States
Full record on ClinicalTrials.gov
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