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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
Carilion Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Distal Radius Fracture focused on measuring Blood Flow Restriction

Eligibility Criteria

50 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

First Posted
May 25, 2022
Last Updated
May 25, 2022
Sponsor
Carilion Clinic
Collaborators
Virginia Polytechnic Institute and State University
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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:
PubMed Identifier
30725601
Citation
Corsino CB, Reeves RA, Sieg RN. Distal Radius Fractures. 2023 Aug 8. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2023 Jan-. Available from http://www.ncbi.nlm.nih.gov/books/NBK536916/
Results Reference
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Citation
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PubMed Identifier
33892883
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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PubMed Identifier
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Citation
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Citation
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PubMed Identifier
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Citation
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Results Reference
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BFR Therapy Following DRF

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