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Efficacy Study of an Unloading Brace for Knee Osteoarthritis

Primary Purpose

Osteoarthritis of the Knee

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Breg Fusion Unloading Brace
Sponsored by
Andrews Research & Education Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Osteoarthritis of the Knee focused on measuring knee osteoarthritis unicompartmental unloading brace

Eligibility Criteria

30 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 30-80.
  • History of medial unicompartmental knee pain > 3 months duration (medial compartment only).
  • Narrowing of medial joint space < one half of lateral compartment
  • Varus deformity no greater than 80
  • Mild to moderate limitation in Activities of Daily Living (ADL's) and/or recreational activities.
  • Must read and understand English language and demonstrate the ability and willingness to follow the protocol and complete the questionnaires and diaries.
  • Manual dexterity sufficient to perform all tasks required of study participants.
  • Willingness to wear the brace a minimum of 4 hours per day.

Exclusion Criteria:

  • Arthritides other than osteoarthritis.
  • Previous high tibial osteotomy of the affected knee.
  • Previous surgery of affected knee other than diagnostic arthroscopy with joint debridement, soft tissue reconstruction, menisectomy.
  • Fixed flexion deformities / limitations >10 degrees as compared to the contralateral limb.
  • Flexion limitation > 20 degrees.
  • Significant soft tissue compromise preventing long-term brace use.
  • Peripheral vascular disease or other neurovascular complaints.
  • Leg-length discrepancy > 2cm.

Sites / Locations

  • Andrews Institute for Orthopaedics & Sports Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control Group

Experimental Group

Arm Description

This group receives no experimental bracing intervention in the study.

This group will receive the Breg Fusion Osteoarthritis Knee Unloading Brace to wear for a determined amount of time per study protocol for the treatment of osteoarthritis pain.

Outcomes

Primary Outcome Measures

Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain Score
The Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire will be administered to collect patient reported outcomes as they relate to pain, function, and quality of life. The pain scale range is 0-10 with lower scores indicating less pain.

Secondary Outcome Measures

Full Information

First Posted
May 27, 2014
Last Updated
October 2, 2019
Sponsor
Andrews Research & Education Foundation
Collaborators
BREG, Inc
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1. Study Identification

Unique Protocol Identification Number
NCT02150057
Brief Title
Efficacy Study of an Unloading Brace for Knee Osteoarthritis
Official Title
Efficacy of Medial Compartment Unloading Brace Use for Osteoarthritis of the the Knee: A Prospective Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Andrews Research & Education Foundation
Collaborators
BREG, Inc

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Subjects with symptomatic unicompartmental osteoarthritis of the knee will be invited to participate in this randomized study. Subjects will be assigned to either a Fusion Osteoarthritis Knee Brace group, or a control group that does not wear a brace. It is hypothesized that use of the Fusion Osteoarthritis Knee Brace will have a better outcome on osteoarthritis knee pain and quality of life compared to those who do not receive bracing intervention.
Detailed Description
This investigation will recruit 72 subjects from the clinical population of the investigators with symptomatic unicompartmental osteoarthritis of the medial compartment of the knee who meet the inclusion criteria of the investigation. Subjects who meet the recruitment conditions will be prospectively randomized into one of two treatment groups for 6 month evaluation: Fusion Osteoarthritis Knee Brace No brace group Inclusion Criteria: Age 30-80. History of medial unicompartmental knee pain > 3 months duration (medial compartment only). Narrowing of medial joint space < one half of lateral compartment Varus deformity no greater than 80 Mild to moderate limitation in Activities of Daily Living (ADL's) and/or recreational activities. Must read and understand English language and demonstrate the ability and willingness to follow the protocol and complete the questionnaires and diaries. Manual dexterity sufficient to perform all tasks required of study participants. Willingness to wear the brace a minimum of 4 hours per day. Exclusion Criteria: Arthritides other than osteoarthritis. Previous high tibial osteotomy of the affected knee. Previous surgery of affected knee other than diagnostic arthroscopy with joint debridement, soft tissue reconstruction, menisectomy. Fixed flexion deformities / limitations >10 degrees as compared to the contralateral limb. Flexion limitation > 20 degrees. Significant soft tissue compromise preventing long-term brace use. Peripheral vascular disease or other neurovascular complaints

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis of the Knee
Keywords
knee osteoarthritis unicompartmental unloading brace

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Subjects who meet the recruitment conditions will be prospectively randomized into one of two treatment groups for 6 month evaluation: Breg Fusion Osteoarthritis Knee Brace No brace group Both groups will be allowed to continue standard conservative treatment of osteoarthritis including anti-inflammatory medications, home exercises and joint supplements.
Masking
Care Provider
Masking Description
Two orthopedic surgeons will blindly grade the osteoarthritis and calculate the mechanical axis and knee angles. The two surgeons' measurements will be averaged. One surgeon's measurements will be repeated to determine intra-observer reliability.
Allocation
Randomized
Enrollment
51 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
This group receives no experimental bracing intervention in the study.
Arm Title
Experimental Group
Arm Type
Active Comparator
Arm Description
This group will receive the Breg Fusion Osteoarthritis Knee Unloading Brace to wear for a determined amount of time per study protocol for the treatment of osteoarthritis pain.
Intervention Type
Device
Intervention Name(s)
Breg Fusion Unloading Brace
Other Intervention Name(s)
Breg Fusion Osteoarthritis Knee Unloading Brace
Intervention Description
This group is assigned to wear an unloading brace and report pain and quality of life by completion of a pain diary and related questionnaires.
Primary Outcome Measure Information:
Title
Knee Injury and Osteoarthritis Outcome Score (KOOS) Pain Score
Description
The Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire will be administered to collect patient reported outcomes as they relate to pain, function, and quality of life. The pain scale range is 0-10 with lower scores indicating less pain.
Time Frame
Baseline, 6 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 30-80. History of medial unicompartmental knee pain > 3 months duration (medial compartment only). Narrowing of medial joint space < one half of lateral compartment Varus deformity no greater than 80 Mild to moderate limitation in Activities of Daily Living (ADL's) and/or recreational activities. Must read and understand English language and demonstrate the ability and willingness to follow the protocol and complete the questionnaires and diaries. Manual dexterity sufficient to perform all tasks required of study participants. Willingness to wear the brace a minimum of 4 hours per day. Exclusion Criteria: Arthritides other than osteoarthritis. Previous high tibial osteotomy of the affected knee. Previous surgery of affected knee other than diagnostic arthroscopy with joint debridement, soft tissue reconstruction, menisectomy. Fixed flexion deformities / limitations >10 degrees as compared to the contralateral limb. Flexion limitation > 20 degrees. Significant soft tissue compromise preventing long-term brace use. Peripheral vascular disease or other neurovascular complaints. Leg-length discrepancy > 2cm.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Roger Ostrander, MD
Organizational Affiliation
Andrews Institute for Orthopaedics & Sports Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Andrews Institute for Orthopaedics & Sports Medicine
City
Gulf Breeze
State/Province
Florida
ZIP/Postal Code
32561
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Efficacy Study of an Unloading Brace for Knee Osteoarthritis

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