Arthroscopic Surgical Outcome Study In Subjects With Rotator Cuff Tears

Rotator Cuff Clinical Trial

Official title:
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

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

Clinical Trial Details

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

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT02943005` - Post-operative Mobilisation After Rotator Cuff Repair	N/A
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Withdrawn	`NCT02693444` - Comparison of Strength and Constant Score Pre- and Post-Subacromial Injection for Full Thickness Rotator Cuff Tears	N/A
Withdrawn	`NCT00198185` - Cascade PRFM Study: The Evaluation of Cascade Platelet-Rich Fibrin Matrix (PRFM) on Rotator Cuff Healing	Phase 3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