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Arthroscopic Surgical Outcome Study In Subjects With Rotator Cuff Tears

NCT00739947 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 162

Last updated 2021-02-16

No results posted yet for this study

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.

Conditions

  • Rotator Cuff
  • Arthroscopic Surgery

Interventions

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.

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
21 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-13
Primary Completion
2011-07-05
Completion
2011-07-05

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00739947 on ClinicalTrials.gov