Last reviewed · How we verify

NCT00739947

Arthroscopic Surgical Outcome Study In Subjects With Rotator Cuff Tears

Completed Last updated 16 February 2021
What this trial tests

trial testing Observational study of the surgical outcome in Rotator Cuff in 162 participants. Completed in 5 July 2011.

Timeline
13 October 2008
Primary endpoint
5 July 2011
5 July 2011

Quick facts

Lead sponsorPfizer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment162
Start date13 October 2008
Primary completion5 July 2011
Estimated completion5 July 2011
Sites37 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Pfizer — full company profile →

Who can join

Adults 21 to 75, any sex, with Rotator Cuff or Arthroscopic Surgery. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. An Evaluation of the Rotator Cuff Repair Research Pipeline.
    Checketts JX, Scott J, Gordon J, Jones J, et al · · 2018 · cited 9× · PMID 30480012 · DOI 10.1177/2325967118805731

Verify or expand the search:

Other recruiting trials for Rotator Cuff

Currently open trials in the same condition.

Other Pfizer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00739947.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing