Evaluation the Operative Procedure Among Patients That Suffer From Tear of the Distal Tendon of the Biceps

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2011 by Hadassah Medical Organization.
Recruitment status was  Not yet recruiting
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
First received: April 27, 2011
Last updated: December 25, 2011
Last verified: December 2011

Background: rupture of the distal tendon in biceps muscle is a rare injury. The state of the art treatment is surgical procedure.

Objective: Evaluation of the Surgical procedure among patients that suffered from Methods: The investigators will review files from 2003-2010 of patients that gone through the operation. The investigators will record pre-operation and post-operation process including complications and rehabilitation. The investigators will invite them to the clinic for exams, clinical questionnaires.

Condition Intervention
Biceps Tendon Rupture
Procedure: tear of the distal tendon in the biceps muscle

Study Type: Observational
Study Design: Observational Model: Case-Crossover
Time Perspective: Retrospective

Resource links provided by NLM:

Further study details as provided by Hadassah Medical Organization:

Groups/Cohorts Assigned Interventions
surgery, biceps tear Procedure: tear of the distal tendon in the biceps muscle


Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
men and women that went to surgery due to tear of the distal tendon in the biceps muscle.

Inclusion Criteria:

1.see population description

Exclusion Criteria:

1. Unwillingness to come to the clinic visit.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

Responsible Party: Dr. Shaul Beyth
ClinicalTrials.gov Identifier: NCT01343875     History of Changes
Other Study ID Numbers: beyth03-HMO-CTIL 
Study First Received: April 27, 2011
Last Updated: December 25, 2011
Health Authority: Israel: Ministry of Health

ClinicalTrials.gov processed this record on May 05, 2016