Distal Radius Fracture Clinical Trial
Official title:
Utilizing Blood Flow Restriction Therapy Following ORIF Treated Distal Radius Fractures
NCT number | NCT05396521 |
Other study ID # | IRB-21-1514 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | May 26, 2022 |
Est. completion date | April 1, 2025 |
Verified date | May 2022 |
Source | Carilion Clinic |
Contact | Evan P Sandefur |
Phone | 262-893-2786 |
evansandefur[@]vt.edu | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study's goal is to evaluate whether blood flow restriction supplemented therapy is a superior therapy compared to traditional standard of care while recovering from a surgery that repairs distal radius fractures. In order to measure this, subjects will be randomly assigned to either the traditional therapy group (with standard of care) or a blood flow restriction supplemented therapy group. All patients involved in this study will have had a distal radius fracture that is repaired with a technique called volar plating and the procedure will be done via an open technique. All subjects will be asked to fill out questionnaires that assess their pain and wrist functionality throughout the course of the study. These measurements will help understand whether the supplemented therapy is effective at reducing pain and improving functionality for patients who are recovering from this injury.
Status | Recruiting |
Enrollment | 78 |
Est. completion date | April 1, 2025 |
Est. primary completion date | May 26, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 50 Years to 75 Years |
Eligibility | Inclusion Criteria: - Outpatients undergoing distal radius fracture open reduction internal fixation using volar plating (CPT 25607, 25608, and 25609) - Age 50 - 75 - Fall onto outstretched hand injury Exclusion Criteria: - High energy mechanism - Fall from an elevated position greater than 12 inches - Motor vehicle collision - Any activity involving a powered vehicle (scooter, car, truck, ATV, motorcycle, tractor, etc.) - any concomitant injury to the affected limb - Bilateral distal radius fracture - Revision procedures - Worker's compensation status - Non-English speaking - No Internet Access - Inability to provide informed consent - Patients with known lymphovascular disorders, including peripheral arterial disease (PAD), prior deep vein thrombosis (DVT) or chronic lymphedema - Patients with known genetic or other hypercoagulability disorders including those on long-term anticoagulation or anti-platelet therapy (other than prophylactic aspirin) - Uncontrolled hypertension - Patients with dialysis catheters or AV fistula - Any other medical condition that affects the risk profile of the patient or that affects the normal physiologic function of the circulatory system of the extremities, based on sole discretion and medical judgement of the Primary Investigator |
Country | Name | City | State |
---|---|---|---|
United States | Carilion Clinic | Roanoke | Virginia |
Lead Sponsor | Collaborator |
---|---|
Carilion Clinic | Virginia Polytechnic Institute and State University |
United States,
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Corsino CB, Reeves RA, Sieg RN. Distal Radius Fractures. 2022 May 1. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK536916/ — View Citation
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Kooner P, Grewal R. Is Therapy Needed After Distal Radius Fracture Treatment, What Is the Evidence? Hand Clin. 2021 May;37(2):309-314. doi: 10.1016/j.hcl.2021.02.012. Review. — View Citation
Loenneke JP, Fahs CA, Wilson JM, Bemben MG. Blood flow restriction: the metabolite/volume threshold theory. Med Hypotheses. 2011 Nov;77(5):748-52. doi: 10.1016/j.mehy.2011.07.029. Epub 2011 Aug 12. — View Citation
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Pope D, Tang P. Carpal Tunnel Syndrome and Distal Radius Fractures. Hand Clin. 2018 Feb;34(1):27-32. doi: 10.1016/j.hcl.2017.09.003. Review. — View Citation
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | PROMIS Pain interference SF V1.1 | 3 months | ||
Primary | PRWE | 3 months |
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