Actively Recruiting
Return to Play After ACL Reconstruction With Bone Marrow Aspirate, DBM, and an Internal Brace
Led by Marshall University · Updated on 2024-03-05
450
Participants Needed
1
Research Sites
226 weeks
Total Duration
On this page
Sponsors
M
Marshall University
Lead Sponsor
A
Arthrex, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The Investigators are studying the effect of an ACL reconstruction on return to play by capturing outcome measures and biomechanics information.
CONDITIONS
Official Title
Return to Play After ACL Reconstruction With Bone Marrow Aspirate, DBM, and an Internal Brace
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 14 to 26 years old
- Skeletally mature patients with an ACL deficient knee planning ACL reconstructive surgery using autograft augmentation
- Tanner stage 5 confirmed by posteroanterior left hand x-ray to verify bone age and skeletal maturity
- Patients with meniscal or chondral pathology included if not excluded by other criteria; such pathology treated during ACL reconstruction and recorded
- Understanding of study purpose and ability to provide written informed consent
You will not qualify if you...
- Patients undergoing multi-ligament surgery (MCL, PCL, LCL, PMC, or PLC repair or reconstruction)
- Patients with previous ACL reconstructive surgery
- Pregnant or nursing patients
- Patients with current infection at the operative site
- Any condition or personal issue deemed by the surgeon to negatively affect study outcome
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Marshall University
Huntington, West Virginia, United States, 25755
Actively Recruiting
Research Team
C
chad d lavender, md
CONTACT
K
Kara Cipriani, NP
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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