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Massive Rotator Cuff Tear Reconstruction

NCT03425500 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2023-08-29

No results posted yet for this study

Summary

To compare bridging reconstruction to superior capsular reconstruction using human dermal allograft augmentation for repair of massive rotator cuff tears.

Conditions

  • Rotator Cuff Tear Arthropathy

Interventions

PROCEDURE

Bridging Rotator Cuff Reconstruction

Bridging Rotator Cuff Reconstruction of massive rotator cuff tear using a GRAFTJACKET™ allograft

PROCEDURE

Superior Capsular Reconstruction

Superior Capsular Reconstruction of massive rotator cuff tear

DEVICE

GRAFTJACKET™ allograft

The acellular human dermal allograft in used in the bridging rotator cuff reconstruction

Sponsors & Collaborators

  • Nova Scotia Health Authority

    lead OTHER

Principal Investigators

  • Ivan H Wong, MD · Nova Scotia Health Authority

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2025-07-31
Completion
2025-08-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03425500 on ClinicalTrials.gov