Trials / Completed
CompletedNCT00739947
Arthroscopic Surgical Outcome Study In Subjects With Rotator Cuff Tears
A PROSPECTIVE STUDY TO EVALUATE SURGICAL OUTCOMES IN SUBJECTS WITH FULL-THICKNESS ROTATOR CUFF TEARS TREATED BY MEANS OF A DOUBLE-ROW ARTHROSCOPIC REPAIR.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 162 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 21 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This is an observational study that involves subjects with full-thickness rotator cuff tears treated by means of arthroscopy surgical repair, also known as arthroscopic surgery. The primary objective of this study is to observe the timing and rate of tendon retear in those subjects.
Detailed description
Subjects will be recruited from each surgeon's surgical practice. They will be reviewed to assure they meet all eligibility criteria prior to enrolling them into the study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Observational study of the surgical outcome | Subjects return for 7 follow-up visits following arthroscopic repair of their rotator cuff. During the follow-up visits subjects undergo imaging with MRI and ultrasound. |
Timeline
- Start date
- 2008-10-13
- Primary completion
- 2011-07-05
- Completion
- 2011-07-05
- First posted
- 2008-08-22
- Last updated
- 2021-02-16
Locations
37 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00739947. Inclusion in this directory is not an endorsement.