ACTIVE_NOT_RECRUITING

Connective Tissue Matrix for Rotator Cuff Tendinopathy

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this research study is to determine if the effectiveness of a single injection of CTM Boost in the treatment of patients with rotator cuff tendinopathy (RCT) is as effective as a single injection of platelet rich plasma (PRP) in reducing the symptoms of RCT.

Official Title

Connective Tissue Matrix (CTM) for Rotator Cuff Tendinopathy: A Randomized Controlled Trial

Quick Facts

Study Start:2023-12-04
Study Completion:2028-01-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06160427

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients aged 18-80 years old with rotator cuff tendinopathy
  2. * A PRP or CTM-type injection was determined by the clinician to be the proper medical treatment course and patient is willing to undergo the injection
  1. * Patients with adhesive capsulitis
  2. * Patients with acromio-clavicular joint impingement, retracted tears, significant labral lesions or significant glenohumeral arthrosis
  3. * Patients with joint instability
  4. * History of shoulder surgery or corticosteroid injection in the past 3 months
  5. * Patients with any medical conditions that affect healing, such as end-stage renal disease or uncontrolled diabetes

Contacts and Locations

Principal Investigator

Patrick Demeo, MD
PRINCIPAL_INVESTIGATOR
Allegheny Health Network

Study Locations (Sites)

Allegheny Health Network Allegheny General Hospital
Pittsburgh, Pennsylvania, 15212
United States
Allegheny Health Network Federal North Medical Office Building
Pittsburgh, Pennsylvania, 15212
United States
AHN Wexford Health & Wellness Pavilion
Wexford, Pennsylvania, 15090
United States
AHN Wexford Hospital
Wexford, Pennsylvania, 15090
United States

Collaborators and Investigators

Sponsor: Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

  • Patrick Demeo, MD, PRINCIPAL_INVESTIGATOR, Allegheny Health Network

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-12-04
Study Completion Date2028-01-15

Study Record Updates

Study Start Date2023-12-04
Study Completion Date2028-01-15

Terms related to this study

Keywords Provided by Researchers

  • rotator cuff tendinopathy

Additional Relevant MeSH Terms

  • Tendinopathy
  • Shoulder Pain
  • Rotator Cuff Tendinitis
  • Rotator Cuff Tendinosis