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NCT06287853

Tapestry Rotator Cuff Repair PMCF

Suspended Last updated 21 November 2025
What this trial tests

trial testing Tapestry Biointegrative Implant in Rotator Cuff Tears in 170 participants. Suspended.

Timeline
28 December 2026
Primary endpoint
30 December 2030
30 December 2030

Quick facts

Lead sponsorZimmer Biomet
StatusSuspended
Study typeOBSERVATIONAL
Enrollment170
Start date28 December 2026
Primary completion30 December 2030
Estimated completion30 December 2030
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Zimmer Biomet — full company profile →

Who can join

21 and older, any sex, with Rotator Cuff Tears or Rotator Cuff Injuries. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study design is a prospective, multi-center, single-arm, non-randomized, and noncontrolled post market clinical follow-up study involving orthopedic surgeons skilled in arthroscopic rotator cuff repair as determined by the Sponsor.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Rotator Cuff Tears

Currently open trials in the same condition.

Other Zimmer Biomet trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06287853.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing