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NCT06160427 · ClinicalTrials.gov registry record · Phase 4

Connective Tissue Matrix for Rotator Cuff Tendinopathy

A Phase 4 study of Shoulder Pain and Tendinopathy, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

Active
Registry status
Phase 4
Development phase
92
Enrollment target
4
Study locations

NCT06160427: Active Phase 4 study of Shoulder Pain and Tendinopathy, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

NCT06160427 is a Phase 4 study of Shoulder Pain and Tendinopathy that is active but no longer recruiting, run by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute). The registered enrollment target is 92 participants, roughly in line with the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target. The trial reports 4 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06160427, a Phase 4 study of Shoulder Pain and Tendinopathy, is active but no longer recruiting, sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute).

ACTIVE NOT RECRUITING
Registry status
Phase 4
Development phase
92 participants
Enrollment target
4
Study locations

Study Summary

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.

Primary Outcome

Mean Western Ontario Rotator Cuff Index (WORC) Score The WORC has 21 items in four domains, including physical symptoms (10 questions), sports/recreation/work (4 questions), lifestyle (4 questions) and emotions (3 questions). Raw scores range from 0 to 2100, with a higher score indicating decreased quality of life because of pathological condition of the rotator cuff.

Interventions

  • BIOLOGICAL CTM Boost
  • BIOLOGICAL PRP

Study Locations (4)

Pennsylvania

  • Allegheny Health Network Allegheny General Hospital - Pittsburgh
  • Allegheny Health Network Federal North Medical Office Building - Pittsburgh
  • AHN Wexford Health & Wellness Pavilion - Wexford
  • AHN Wexford Hospital - Wexford

Trial Details

FieldValue
Enrollment Target 92 participants
Start Date 2023-12-04
Est. Completion 2028-01-15
Phase Phase 4

What the registry record for NCT06160427 still lists

NCT06160427 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 92 participants, a relatively small participant target, roughly in line with the 98-participant average among 27 other Shoulder Pain trials with a reported enrollment target.

The record links to 4 conditions, with Shoulder Pain appearing as the primary indexed condition, and to 2 interventions - of which CTM Boost is the first listed.

NCT06160427 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06160427 about?

NCT06160427 is a clinical study titled "Connective Tissue Matrix for Rotator Cuff Tendinopathy". 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.

What is the current status of trial NCT06160427?

This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 92 participants. The study started on 2023-12-04. Estimated completion is 2028-01-15.

What conditions does trial NCT06160427 study?

This clinical trial studies the following conditions: Shoulder Pain, Tendinopathy, Rotator Cuff Tendinitis, Rotator Cuff Tendinosis.

What interventions are being tested in trial NCT06160427?

The interventions under investigation include: CTM Boost (BIOLOGICAL), PRP (BIOLOGICAL).

Who is sponsoring clinical trial NCT06160427?

This trial is sponsored by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute), which has 34 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06160427 being conducted?

This trial has 4 study locations across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Shoulder Pain

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06160427's enrollment target sits among peer trials

92 9th of 27 higher than 18 of 27 other Shoulder Pain trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Shoulder Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06160427, the US trial registry maintained by the National Library of Medicine. NCT06160427 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.