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Study identifier: NCT05444465 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Use of the REGENETEN™ Bioinductive Implant System in High Grade Partial-thickness Tears

Condition: Rotator Cuff Injuries  ·  Sponsor: Smith & Nephew, Inc.

PhaseNA
Planned participants234
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of the study is to assess whether the REGENETEN™ Bioinductive Implant allows patients to get back to their everyday activities quicker than if the tendon is repaired by the standard repair technique 'Completion and Repair' for surgically treating partial-thickness rotator cuff tears.

This description comes directly from the study's public registry record.

Talk to the study team

Alice Kitching  ·  +44 (0) 7590001182  ·  alice.kitching@smith-nephew.com

Mary Ozokwere  ·  +1 469-560-0727  ·  Mary.Ozokwere@smith-nephew.com

Always discuss trial participation with your own doctor first.

Locations (20)

Harbin ClinicRome, Georgia, United StatesRecruiting
OrthoIllinois LTDRockford, Illinois, United StatesRecruiting
Sinai Hospital BaltimoreBaltimore, Maryland, United StatesWithdrawn
Cleveland Clinic - Sports HealthGarfield Heights, Ohio, United StatesWithdrawn
University of PittsburghPittsburgh, Pennsylvania, United StatesRecruiting
Texas Orthopedic SpecialistsBedford, Texas, United StatesRecruiting
Houston Methodist The WoodlandsThe Woodlands, Texas, United StatesWithdrawn
Memorial Medical CenterAshland, Wisconsin, United StatesWithdrawn
OrthoSport VictoriaRichmond, Victoria, AustraliaRecruiting
Access OrthopaedicsCalgary, Alberta, CanadaRecruiting
Pan Am ClinicWinnipeg, Manitoba, CanadaRecruiting
Research St. Joseph'sHamilton, Ontario, CanadaRecruiting

+ 8 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05444465