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

ClinicalTrials.gov ID: NCT03985839

Public ClinicalTrials.gov record NCT03985839. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Oct 19, 2026, 11:29 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective Multi-Center Post-Market Clinical Follow-up Study to Evaluate Safety and Performance of the MICRORAPTOR REGENESORB, Knotless REGENESORB and Knotless PEEK Suture Anchors (and MINITAPE Sutures) in Shoulder and Hip Arthroscopic Instability Repair

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective, multi-center, PMCF study to evaluate the safety and performance of the MICRORAPTOR REGENESORB suture anchors, MICRORAPTOR Knotless REGENESORB suture anchors, and MICRORAPTOR Knotless PEEK suture anchors implanted in 315 subjects needing reattachment of soft tissue to bone.

Study identification

NCT ID: NCT03985839
Recruitment status: Completed
Study type: Observational
Phase: Not listed
Lead sponsor: Smith & Nephew, Inc.; Industry
Enrollment: 298 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range: 12 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Aug 1, 2019 (Actual)
Primary completion: Aug 8, 2024 (Actual)
Completion: Aug 8, 2024 (Actual)
Last update posted: Jul 13, 2026

2019 – 2024

United States locations

U.S. sites: 12
U.S. states: 9
U.S. cities: 12

Facility	City	State	ZIP	Site status
University of Colorado	Aurora	Colorado	80045	—
Colorado Springs Orthopaedic Group	Colorado Springs	Colorado	80920	—
Holy Cross Orthopedic Institute	Oakland Park	Florida	33334	—
Emory University - Brookhaven	Brookhaven	Georgia	30329	—
Luminis Health Research Institute	Annapolis	Maryland	21401	—
Ohio State University Wexner Medical Center	Columbus	Ohio	43202	—
Oklahoma Sports and Science Orthopedics / The Physician's Group	Oklahoma City	Oklahoma	73114	—
Palmetto/Prisma Health - University of South Carolina Orthopaedics	Columbia	South Carolina	29203	—
Steadman Hawkins Clinic of the Carolinas	Greenville	South Carolina	29615	—
Atlantic Orthopaedic Specialists	Virginia Beach	Virginia	23452	—
Center for Advanced Orthopaedics / Nova Orthopedic & Spine Care	Woodbridge	Virginia	22191	—
Memorial Medical Center	Ashland	Wisconsin	54806	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT03985839, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jul 13, 2026 · Synced Oct 19, 2026

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The complete public registry record, listed eligibility criteria, and available contact information for NCT03985839 live on ClinicalTrials.gov.

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