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NCT01405781 · ClinicalTrials.gov registry record
Functional and Radiographic Outcomes After Shoulder Surgery
A clinical trial, sponsored by University of Utah.
- Completed
- Registry status
- 1,034
- Enrollment target
NCT01405781: Completed study, sponsored by University of Utah.
NCT01405781 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 1,034 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01405781 has completed, sponsored by University of Utah.
- COMPLETED
- Registry status
- 1,034 participants
- Enrollment target
Study Summary
The objective of this study is twofold: First, to determine whether higher levels of pre-operative psychological distress predict worse outcomes after arthroscopic rotator cuff repair; second, to obtain functional outcomes (VAS pain, VAS satisfaction, VAS function, Simple Shoulder Test (SST) and American Shoulder and Elbow Surgeons (ASES) Score), physically examine and perform a radiographic analysis of patients at a minimum of 6 months after reverse total shoulder arthroplasty, total shoulder arthroplasty, arthroscopic scapulothoracic bursectomy, acromioclavicular joint reconstruction and arthroscopic rotator cuff repair.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,034 participants |
| Start Date | 2011-05 |
| Est. Completion | 2024-09-13 |
What the finished NCT01405781 record still lists
NCT01405781 is an observational study that tracks outcomes without assigning an intervention. Its 1,034 participants enrollment target places it among the larger protocols in the corpus.
The record links to 0 conditions, and to 0 interventions.
NCT01405781 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01405781 about?
NCT01405781 is a clinical study titled "Functional and Radiographic Outcomes After Shoulder Surgery". The objective of this study is twofold: First, to determine whether higher levels of pre-operative psychological distress predict worse outcomes after arthroscopic rotator cuff repair; second, to obtain functional outcomes (VAS pain, VAS satisfaction, VAS function, Simple Shoulder Test (SST) and Ame...
What is the current status of trial NCT01405781?
This trial is currently completed. The enrollment target is 1,034 participants. The study started on 2011-05. Estimated completion is 2024-09-13.
Who is sponsoring clinical trial NCT01405781?
This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.
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