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Procedure
Anterior Cruciate Ligament Reconstruction for Anterior Cruciate Ligament Reconstruction
N/A
Waitlist Available
Led By Dana P Piasecki, MD
Research Sponsored by OrthoCarolina Research Institute, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 year post-operative
Awards & highlights
Study Summary
This trial compares two techniques for ACL reconstruction surgery to see which best recreates the original ligament.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 year post-operative
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 year post-operative
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
3D reconstructed CT imaging
Secondary outcome measures
International Knee Documentation Committee (IKDC) Subjective Knee Evaluation
Knee Laxity
Knee injury and Osteoarthritis Outcome Score (KOOS)
Trial Design
3Treatment groups
Active Control
Group I: Hybrid Transtibial TechniqueActive Control1 Intervention
Reconstruction of the ACL using the hybrid transtibial technique
Group II: Transtibial TechniqueActive Control1 Intervention
Reconstruction of the ACL using the transtibial technique.
Group III: Accessory Anteromedial Portal TechniqueActive Control1 Intervention
Reconstruction of the ACL using the accessory anteromedial portal technique
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Who is running the clinical trial?
OrthoCarolina Research Institute, Inc.Lead Sponsor
34 Previous Clinical Trials
5,901 Total Patients Enrolled
Dana P Piasecki, MDPrincipal InvestigatorOrthoCarolina Research Institute, Inc.
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Eligibility Criteria:
This trial includes the following eligibility criteria:- You have had an injury or surgery on the knee opposite to the one being studied.You recently had surgery on a ligament or bone that is not in your knee.Patients must have fully developed bones.You need surgery to fix a torn ACL in your knee, with or without additional surgery to repair or remove part of your meniscus.You have had surgery to reconstruct your anterior cruciate ligament (ACL) in the knee being studied before.
Research Study Groups:
This trial has the following groups:- Group 1: Hybrid Transtibial Technique
- Group 2: Transtibial Technique
- Group 3: Accessory Anteromedial Portal Technique
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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