A Clinical Registry of Orthobiologics Procedures

Status Enrolling by invitation

Clinical Trial 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.

Clinical Trial Description

This Registry was designed to assure that the benefits and knowledge gained by studying clinical outcomes associated with the use of percutaneous orthopedic procedures outweigh the potential risks to the patients. The primary objective of this Registry is to observe the improvements in subject-reported clinical outcomes for these procedures used to treat musculoskeletal disorders. Secondary objectives include evaluating post-treatment complication, adverse events, re-injections, and surgical intervention. Patients receiving percutaneous orthopedic treatments are asked to enroll before receiving treatment and complete a set of baseline questionnaires regarding pain and functionality of the area of the body being treated (i.e. knee, shoulder, spine, etc). Follow-up outcomes are collected at 1 month, 3 months, 6 months, 12 months, 18 months, and annually 2-20 years post-injection. Subjects are withdrawn from the Registry prematurely if a surgical operation occurs. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03011398
Study type	Observational [Patient Registry]
Source	Regenexx, LLC
Contact
Status	Enrolling by invitation
Phase
Start date	February 2016
Completion date	February 2036

View Details

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