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NCT01550952 · ClinicalTrials.gov registry record
Interscalene Dynamometer Pilot Study
A clinical trial of Total Shoulder Arthroplasty, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- 10
- Enrollment target
- 1
- Study location
NCT01550952: Completed study of Total Shoulder Arthroplasty, sponsored by Hospital for Special Surgery, New York.
NCT01550952 is a study of Total Shoulder Arthroplasty that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 10 participants, below the 91-participant average among 3 other Total Shoulder Arthroplasty trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01550952, a study of Total Shoulder Arthroplasty, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- 10 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Anterior deltoid strength as measured by a dynamometer. Percentage change in measure as compared to post-surgery (with post-surgery measure at 0%).
Conditions Studied
Study Locations (1)
New York
- Hospital for Special Surgery - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2011-12 |
| Est. Completion | 2012-02 |
What the finished NCT01550952 record still lists
NCT01550952 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 91-participant average among 3 other Total Shoulder Arthroplasty trials with a reported enrollment target (89% lower).
The record links to 1 condition, with Total Shoulder Arthroplasty appearing as the primary indexed condition, and to 0 interventions.
NCT01550952 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT01550952 about?
NCT01550952 is a clinical study titled "Interscalene Dynamometer Pilot Study". 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, patient...
What is the current status of trial NCT01550952?
This trial is currently completed. The enrollment target is 10 participants. The study started on 2011-12. Estimated completion is 2012-02.
What conditions does trial NCT01550952 study?
This clinical trial studies the following conditions: Total Shoulder Arthroplasty.
Who is sponsoring clinical trial NCT01550952?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01550952 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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