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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00762580
Other study ID # 060109
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2006
Est. completion date January 11, 2024

Study information

Verified date January 2024
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to find which patients will improve with the nonsurgical treatment of physical therapy for the treatment of rotator cuff tears.


Description:

Rotator cuff tears are found in up to 40% of people over the age of 50 with the prevalence increasing with age. While most people remain asymptomatic, it is unknown why some develop symptoms. In symptomatic patients, surgical repair of a torn rotator cuff fails in 30-50% of patients, yet the majority of patients have a significant reduction pain despite failure of the repair. Nonoperative treatment has reported successful outcomes in 25-82% of patients yet it is not known which patient-related features predict success with nonoperative treatment. The general aim of this research effort is to identify patient features (historical information, physical examination findings, and MRI-based pathology) that would predict success (defined by reduction in visual analog pain scale, and patient satisfaction) with the nonoperative treatment of rotator cuff tears. The proposed study design is a prospective cohort study of patients with rotator cuff tears who will follow a standard physical therapy program derived from an evidence based medicine (EBM) systematic review of Level 1 and Level 2 studies. Study the effect of historical information on predicting success (as determined by pain relief and patient satisfaction) of nonoperative treatment using the EBM based physical therapy program in treating patients with rotator cuff tears. Study the effect of physical examination findings on predicting success of a nonoperative treatment using the EBM-based physical therapy program in treating patients with rotator cuff tears. Study the effect of the severity of the rotator cuff pathology (using standardized magnetic resonance imaging protocols) on predicting success of nonoperative treatment for patients with rotator cuff tears using the EBM-based physical therapy program.


Recruitment information / eligibility

Status Completed
Enrollment 452
Est. completion date January 11, 2024
Est. primary completion date January 11, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: • Patients (18-100 years of age) with MRI findings of a full-thickness rotator cuff tear Note: Criteria to obtain a shoulder MRI to evaluate for rotator cuff tear [Appendix D]: 1. Significant weakness (= 2 points per guidelines above.) 2. ADL pain or night pain >/= 7 on VAS 3. Significant impingement (per guidelines above) + with significant symptoms for = 3 months. Exclusion Criteria: - Acute rotator cuff tears (generally due to a high velocity injury and symptoms of less than one month) - Associated dislocations - Associated fractures - Systemic Rheumatologic disease, i.e. Rheumatoid Arthritis and Systemic Lupus Erythematosis - Patients being treated for bilateral rotator cuff tears simultaneously - Patients unable to complete the forms - Pain from neck or scapula - Previous shoulder surgery - Glenohumeral arthritis (meets = 1 of below criteria) - osteophytes >2mm on humeral head or glenoid - Joint space narrowing with sclerosis or cyst formation seen on true AP or axillary radiographs; - humeral head contacting acromion - Adhesive capsulitis

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Colorado University Sports Medicine Boulder Colorado
United States Ohio State Columbus Ohio
United States Universtiy Of Iowa Iowa City Iowa
United States Shoulder and Elbow Institute, Knoxville Orthopaedic Clinic Knoxville Tennessee
United States Vanderbilt Universtiy Medical Center Nashville Tennessee
United States Hospital for Special Surgery New York New York
United States Department of Orthopaedic Surgery, Washington Universtiy School of Medicine Saint Louis Missouri
United States University of California at San Francisco San Francisco California
United States Sports Medicine & Shoulder Surgery, Orthopedic Institute Sioux Falls South Dakota

Sponsors (10)

Lead Sponsor Collaborator
Vanderbilt University Arthrex, Inc., Hospital for Special Surgery, New York, Knoxville Orthopedic Clinic, Ohio State University, Sports Medicine and Shoulder Surgery Orthopedic Institute, University of California, San Francisco, University of Colorado, Denver, University of Iowa, Washington University School of Medicine

Country where clinical trial is conducted

United States, 

References & Publications (51)

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* Note: There are 51 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Predict successful outcome with an evidence-based, non-operative treatment program by collecting VAS Pain Scale and SANE score. One year
Secondary Predict success of non-operative treatment outcomes with other patient related validated instruments (SF-12, ASES, WORC, Marx Activity Scale) One Year
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