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Safety and Performance of MICRORAPTOR™ Suture Anchors in Shoulder and Hip

← catalyst calendar

NCT03985839 · results posted

Sponsored by Smith & Nephew, Inc. (industry) · SNN — their whole pipeline →.

Phase
Status
Completed
Study type
Observational
Enrollment
298actual
Sites
12
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-25

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2019-08-01actualWhen the study began enrolling
Primary completion2024-08-08actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2024-08-08actualThe whole study's end, after follow-up
First posted2019-06-14actualWhen this record first appeared on the registry
Results posted2026-07-13actualWhen the sponsor posted results to the registry
Record updated2026-07-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Labral Tear, Glenoid
  • Acetabular Labrum Tear
  • Bankart Lesions
  • Anterior Shoulder Instability
  • SLAP Lesion
  • Rotator Cuff Tears

Interventions

  • Device: MICRORAPTOR™ REGENESORB™ Suture Anchor
  • Device: MICRORAPTOR™ Knotless REGENESORB™ Suture Anchor
  • Device: MICRORAPTOR™ Knotless PEEK Suture Anchor

Primary outcome

what the primary-completion date above is the date OF
Repair Failure Rate at 6 Months
measured 6 months

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2021-09-03 · 2.9 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-01-27 · 976 KB · SAP_001.pdf

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