# Prospective Study to Determine the Safety and Effectiveness of a Connective Tissue Allograft Active Matrix (AM) vs. Standard of Care in Arthroscopic Rotator Cuff Repair

> **NCT05894265** · NA · RECRUITING · sponsor: **The University of Texas Health Science Center, Houston** · enrollment: 72 (estimated)

## Conditions studied

- Rotator Cuff Tears

## Interventions

- **OTHER:** ActiveMatrix® Dosage A
- **OTHER:** ActiveMatrix® Dosage B
- **PROCEDURE:** Saline injection

## Key facts

- **NCT ID:** NCT05894265
- **Lead sponsor:** The University of Texas Health Science Center, Houston
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2023-06-14
- **Primary completion:** 2026-08-01
- **Final completion:** 2026-08-01
- **Target enrollment:** 72 (ESTIMATED)
- **Last updated:** 2026-04-29

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05894265

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05894265, "Prospective Study to Determine the Safety and Effectiveness of a Connective Tissue Allograft Active Matrix (AM) vs. Standard of Care in Arthroscopic Rotator Cuff Repair". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT05894265. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*