A Clinical Registry of Orthobiologics Procedures

NCT03011398 · tracked via the Priya Life Science USA tracker

Sponsor

Regenexx, LLC

Phase

Observational

Started

2016-02

Last updated

2025-04-06

Condition(s) studied

Orthopedic Disorder

Investigational drug(s) / intervention(s)

Orthobiologic Procedures

Orthobiologic Procedures: To observe the improvement in subject-reported clinical outcomes for percutaneous orthopedic procedures used to treat musculoskeletal disorders.

Study summary

The purpose of the Registry study is to observe the improvement in subject-reported clinical outcomes for percutaneous orthopedic procedures for treatment of musculoskeletal disorders.

Eligibility

Sex

ALL

Min age

—

Max age

—

Healthy volunteers

Inclusion Criteria: * Candidates must meet ALL of the following: 1. Voluntary signature of the IRB approved Informed Consents, 2. Treated with a Regenexx procedure 3. Have a musculoskeletal condition appropriate for the procedure such as osteoarthritis or internal joint derangement; ligament or tendon injury; intervertebral disc degeneration; protrusion, extrusion, or annular tear; muscle tear Exclusion Criteria: * none

Primary outcome measure(s)

Change in Percent Improvement — 1 month, 3 months, 6 months, 12 months, 18 months and annually 2-20 years post treatment
Mean improvement score, where -100=100% worse from baseline and 100=100% better or improved from baseline

Trial sites (32)

Facility	City	Region
Catalyst Pain Solutions	Phoenix	Arizona
Healthlink Center	Beverly Hills	California
Healthlink Center	Oceanside	California
Healthlink Center	San Rafael	California
Southern California Orthopedic Institute	Thousand Oaks	California
Southern California Orthopedic Institute-Van Nuys	Van Nuys	California
Centeno-Schultz Clinic	Broomfield	Colorado
Regenexx	Broomfield	Colorado
New reGeneration Orthopedics	Sarasota	Florida
Chicago Arthritis	Chicago	Illinois
Orthopedic Stem Cell Resource	Des Plaines	Illinois
Harbor View Medical	Des Moines	Iowa
Bodyworks Musculoskeletal Medicine	Louisville	Kentucky
Total Care-LA	Lafayette	Louisiana
Stem Cell ARTS-MD	Chevy Chase	Maryland
RejuvMedical	Waite Park	Minnesota
New Jersey Sports Medicine	Cedar Knolls	New Jersey
Orthopedic Stem Cell Solutions	Oakhurst	New Jersey
Rehabilitation Center of New Jersey	Wayne	New Jersey
Rehabilitation Center of New York	New York	New York
Beacon Orthopaedics	Cincinnati	Ohio
ProMedica	Toledo	Ohio
RegenOrthoSport	Tulsa	Oklahoma
Columbia Pain Management	Hood River	Oregon
Rehabilitation and Pain Specialists	Pittsburgh	Pennsylvania
Center for Sports Medicine	Springfield	Pennsylvania
RegenOrthoSport	Dallas	Texas
Wasatch Pain Solutions	South Jordan	Utah
Vermont Regenerative Medicine	Winooski	Vermont
Stem Cell ARTS-VA	McLean	Virginia
Nepean Specialist Sports Medicine	Kingswood	New South Wales
RegenOrthoSport	Hyderabad	Telangana

More Regenexx, LLC trials in the USA

Use of Bone Marrow Concentrate for Treatment of Alar, Accessory, and Transverse Ligament Injuries Recruiting

Trial for Treating Painful Degenerative Disc Disease Recruiting

Other trials for the same condition

CERAMENT™| Bone Void Filler Device Registry Recruiting

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03011398 on ClinicalTrials.gov ↗ ← All trials in the USA