BFR Therapy Following DRF
Primary Purpose
Distal Radius Fracture
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Blood Flow Restriction
Standard of Care Physical Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Distal Radius Fracture focused on measuring Blood Flow Restriction
Eligibility Criteria
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
Sites / Locations
- Carilion ClinicRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard of Care
Blood Flow Restriction Supplemented
Arm Description
Outcomes
Primary Outcome Measures
PROMIS Pain interference SF V1.1
PRWE
Secondary Outcome Measures
Full Information
NCT ID
NCT05396521
First Posted
May 25, 2022
Last Updated
May 25, 2022
Sponsor
Carilion Clinic
Collaborators
Virginia Polytechnic Institute and State University
1. Study Identification
Unique Protocol Identification Number
NCT05396521
Brief Title
BFR Therapy Following DRF
Official Title
Utilizing Blood Flow Restriction Therapy Following ORIF Treated Distal Radius Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 26, 2022 (Actual)
Primary Completion Date
May 26, 2024 (Anticipated)
Study Completion Date
April 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Carilion Clinic
Collaborators
Virginia Polytechnic Institute and State University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Distal Radius Fracture
Keywords
Blood Flow Restriction
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
78 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of Care
Arm Type
Active Comparator
Arm Title
Blood Flow Restriction Supplemented
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Blood Flow Restriction
Intervention Description
Group 2 (experimental) will receive standard of care physical therapy to be done with blood flow restriction therapy (BFR). This method includes standard of care physical therapy while occluding blood flow.
Intervention Type
Other
Intervention Name(s)
Standard of Care Physical Therapy
Intervention Description
Group 1 (Control) will receive standard of care physical therapy.
Primary Outcome Measure Information:
Title
PROMIS Pain interference SF V1.1
Time Frame
3 months
Title
PRWE
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Evan P Sandefur
Phone
262-893-2786
Email
evansandefur@vt.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Peter J Apel, MD, PhD
Email
pjapel@carilionclinic.org
Facility Information:
Facility Name
Carilion Clinic
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24014
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Darren T Hackley
Phone
540-613-2972
Email
dthackley@carilionclinic.org
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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30725601
Citation
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Citation
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.
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BFR Therapy Following DRF
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