The BEAR III Trial for Bridge-Enhanced ACL (Anterior Cruciate Ligament) Restoration
Primary Purpose
Anterior Cruciate Ligament Injury, Anterior Cruciate Ligament Rupture
Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Bridge-Enhanced ACL Restoration (BEAR)
Sponsored by
About this trial
This is an interventional treatment trial for Anterior Cruciate Ligament Injury
Eligibility Criteria
Inclusion Criteria: ACL tear, within 50 days of injury, at least 5% of the ACL attached to the tibia.
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Exclusion Criteria: Prior surgery on the affected knee, history of knee infection, use of tobacco, use of corticosteroid, chemotherapy, allergy to bovine products or gelatin, history of anaphylaxis, BMI over 35, moderate osteoarthritis.
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Sites / Locations
- Scripps Health
- Florida Orthopedic Institute
- Emory University School Of Medicine
- Ochsner Sports Medicine Institute
- MedStar Health Surgery Center of Timonium
- Boston Children's Hospital
- Virtua Health
- Cynthia Chrostek
- Orthopedic Institute of Sioux Falls
- UT Southwestern
- Inova Sports Medicine
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Bridge-Enhanced ACL Restoration (BEAR)
Arm Description
The BEAR technique involves surgically placing an absorbable implant (the BEAR Implant) between the torn ends of the ACL, providing a scaffold for the ligament ends to grow into
Outcomes
Primary Outcome Measures
International Knee Documentation Committee Subjective Score (IKDC) (Survey)
This is a survey patients complete about how their knee is feeling and functioning. Range is 0 to 100, with 100 indicating no problems and 0 indicating extreme problems.
International Knee Documentation Committee Objective Score (IKDC) (Physical Exam)
This is an examination performed of the knee. Scores are one of four measures: A (Normal), B (Nearly Normal), C (Abnormal) and D (Severely Abnormal). A is the best outcome and D is the worst.
Secondary Outcome Measures
Knee Injury and Osteoarthritis Score (KOOS) questionnaire
This is a survey with 5 subscales (Pain, Symptoms, Function in Daily Living, Function in Sport and Recreation, and Knee Related Quality of Life). The range of each subscale is 0 to 100, with 100 indicating no problems and 0 indicating extreme problems. The subscales are reported individually and not combined.
Repair Failure
The number of times patients develop recurrent knee stability and require another ACL surgery.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03348995
Brief Title
The BEAR III Trial for Bridge-Enhanced ACL (Anterior Cruciate Ligament) Restoration
Official Title
A Prospective Cohort Clinical Trial Evaluating Age as a Risk Factor for Poor Outcomes of Bridge-Enhanced ACL Restoration (BEAR)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 17, 2018 (Actual)
Primary Completion Date
April 17, 2024 (Anticipated)
Study Completion Date
April 17, 2034 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Miach Orthopaedics
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Bridge-Enhanced ACL Restoration (BEAR) is a new procedure being developed to treat patients with ACL injuries. In the BEAR procedure, an implant is placed between the torn ends of the ACL and the patient's own blood is added to the implant to stimulate ligament healing. We propose the current study to determine if older patients do better than younger patients (or vice versa) with this procedure. This is a cohort study designed to determine if age is a risk factor for a worse outcome after a bridge-enhanced ACL repair (BEAR) as defined by an 11.5 point difference on the IKDC Subjective or Objective Knee Evaluation score at two years after surgery. Additional objectives are to determine the effect of age on safety outcomes including infection, graft rejection, and need for further surgical procedures.
Detailed Description
The BEAR III study is a cohort study designed to determine if age is a risk factor for a worse outcome after a bridge-enhanced ACL restoration (BEAR) as defined by an 11.5 point difference on the IKDC Subjective or Objective Knee Evaluation score at two years after surgery. Additional objectives are to determine the effect of age on safety outcomes including infection, graft rejection, and need for further surgical procedures.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Injury, Anterior Cruciate Ligament Rupture
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Cohort Study
Masking
None (Open Label)
Allocation
N/A
Enrollment
250 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Bridge-Enhanced ACL Restoration (BEAR)
Arm Type
Experimental
Arm Description
The BEAR technique involves surgically placing an absorbable implant (the BEAR Implant) between the torn ends of the ACL, providing a scaffold for the ligament ends to grow into
Intervention Type
Device
Intervention Name(s)
Bridge-Enhanced ACL Restoration (BEAR)
Intervention Description
In the BEAR Procedure, surgery is performed to sew the ACL back together and a scaffold is placed between the torn ends at the time of repair.
Primary Outcome Measure Information:
Title
International Knee Documentation Committee Subjective Score (IKDC) (Survey)
Description
This is a survey patients complete about how their knee is feeling and functioning. Range is 0 to 100, with 100 indicating no problems and 0 indicating extreme problems.
Time Frame
Time points up to two years
Title
International Knee Documentation Committee Objective Score (IKDC) (Physical Exam)
Description
This is an examination performed of the knee. Scores are one of four measures: A (Normal), B (Nearly Normal), C (Abnormal) and D (Severely Abnormal). A is the best outcome and D is the worst.
Time Frame
Time points up to two years.
Secondary Outcome Measure Information:
Title
Knee Injury and Osteoarthritis Score (KOOS) questionnaire
Description
This is a survey with 5 subscales (Pain, Symptoms, Function in Daily Living, Function in Sport and Recreation, and Knee Related Quality of Life). The range of each subscale is 0 to 100, with 100 indicating no problems and 0 indicating extreme problems. The subscales are reported individually and not combined.
Time Frame
Time points up to two years
Title
Repair Failure
Description
The number of times patients develop recurrent knee stability and require another ACL surgery.
Time Frame
Two years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ACL tear, within 50 days of injury, at least 5% of the ACL attached to the tibia.
-
Exclusion Criteria: Prior surgery on the affected knee, history of knee infection, use of tobacco, use of corticosteroid, chemotherapy, allergy to bovine products or gelatin, history of anaphylaxis, BMI over 35, moderate osteoarthritis.
-
Facility Information:
Facility Name
Scripps Health
City
San Diego
State/Province
California
ZIP/Postal Code
92121
Country
United States
Facility Name
Florida Orthopedic Institute
City
Tampa
State/Province
Florida
ZIP/Postal Code
33637
Country
United States
Facility Name
Emory University School Of Medicine
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30329
Country
United States
Facility Name
Ochsner Sports Medicine Institute
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70121
Country
United States
Facility Name
MedStar Health Surgery Center of Timonium
City
Lutherville
State/Province
Maryland
ZIP/Postal Code
21093
Country
United States
Facility Name
Boston Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Virtua Health
City
Marlton
State/Province
New Jersey
ZIP/Postal Code
08053
Country
United States
Facility Name
Cynthia Chrostek
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Facility Name
Orthopedic Institute of Sioux Falls
City
Sioux Falls
State/Province
South Dakota
ZIP/Postal Code
57105
Country
United States
Facility Name
UT Southwestern
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Facility Name
Inova Sports Medicine
City
Fairfax
State/Province
Virginia
ZIP/Postal Code
22031
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The BEAR III Trial for Bridge-Enhanced ACL (Anterior Cruciate Ligament) Restoration
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