Repair of Subscapularis Tear :Clinical Results and MRI Analysis

This study is currently recruiting participants.
Verified June 2012 by Peking University Third Hospital
Sponsor:
Information provided by (Responsible Party):
Lin Lin, Peking University Third Hospital
ClinicalTrials.gov Identifier:
NCT01752088
First received: December 14, 2012
Last updated: December 18, 2012
Last verified: June 2012
  Purpose

This study is to evaluate the magnetic resonance imaging (MRI) and clinical results of arthroscopic repair of subscapularis tears


Condition
Rupture Subscapularis Tendon

Study Type: Observational [Patient Registry]
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Target Follow-Up Duration: 2 Years
Official Title: Arthroscopic Repair of Subscapularis Tear :Clinical Results and MRI Analysis

Further study details as provided by Peking University Third Hospital:

Primary Outcome Measures:
  • Clinical results and MRI analysis [ Time Frame: 2 year ] [ Designated as safety issue: No ]
    ROM UCLA Constant ASES VAS MRI


Estimated Enrollment: 60
Study Start Date: June 2012
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: June 2013 (Final data collection date for primary outcome measure)
Detailed Description:

ROM UCLA Constant ASES VAS MRI Goutallier

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Patients suffering from rotator cuff injury will be scheduled for an arthroscopic procedure

Criteria

Inclusion Criteria:

- Patients suffering from rotator cuff injury scheduled for an arthroscopic procedure. A partial- or full-thickness subscapu-laris tendon tear

Exclusion Criteria:

- revision repairs or open repairs.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01752088

Contacts
Contact: Lin Lin, MD. PhD 86-10-82267019 simon.lin2003@163.com

Locations
China, Beijing
Peking University Third Hospital Recruiting
Beijing, Beijing, China, 100191
Contact: lin lin, MD, PhD    86-10-82267019    simon.lin2003@163.com   
Principal Investigator: lin lin, MD, PhD         
Sponsors and Collaborators
Peking University Third Hospital
Investigators
Study Chair: Guoqing Cui, MD Peking University Third Hospital
  More Information

Publications:
Responsible Party: Lin Lin, Dr., Peking University Third Hospital
ClinicalTrials.gov Identifier: NCT01752088     History of Changes
Other Study ID Numbers: SSC2012
Study First Received: December 14, 2012
Last Updated: December 18, 2012
Health Authority: China: Food and Drug Administration

Keywords provided by Peking University Third Hospital:
apularis, MRI clinical, results

Additional relevant MeSH terms:
Rupture
Wounds and Injuries

ClinicalTrials.gov processed this record on April 15, 2014