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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00739947
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date October 13, 2008
Completion date July 5, 2011

See also
  Status Clinical Trial Phase
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Recruiting NCT03752034 - Muscle Fiber Fragments for Improved Function of Rotator Cuff Musculature Following Rotator Cuff Repair N/A
Withdrawn NCT02693444 - Comparison of Strength and Constant Score Pre- and Post-Subacromial Injection for Full Thickness Rotator Cuff Tears N/A
Withdrawn NCT00198185 - Cascade PRFM Study: The Evaluation of Cascade Platelet-Rich Fibrin Matrix (PRFM) on Rotator Cuff Healing Phase 3
Active, not recruiting NCT04552119 - Safety of Treatment of Shoulder Repair
Recruiting NCT05668533 - Intrscalene Block Versus Pericapsular Nerve Group Block for Arthroscopic Shoulder Surgery N/A
Completed NCT01122745 - Single Shot vs Continuous Interscalene Block for Rotator Cuff Repair N/A