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Procedure
ACLR with lateral extra-articular tenodesis for Ruptured Achilles Tendon
N/A
Waitlist Available
Led By Laith Jazrawi, MD
Research Sponsored by NYU Langone Health
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial is testing whether adding a surgery to fix a torn ACL improves the healing process, by comparing MRI results of those who had the extra surgery to those who did not.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Determine if ACLR supplementation with LET results in superior MRI findings relative to ACLR alone
Secondary outcome measures
Graft Failure
Trial Design
2Treatment groups
Experimental Treatment
Group I: ACLR with lateral extra-articular tenodesisExperimental Treatment1 Intervention
All LETs will be performed in a standardized fashion using the modified Lameire technique.
Group II: ACLRExperimental Treatment1 Intervention
All patients will undergo an anatomic ACLR via a standardized fashion using BTB autogaft graft.
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Who is running the clinical trial?
NYU Langone HealthLead Sponsor
1,369 Previous Clinical Trials
840,635 Total Patients Enrolled
Laith Jazrawi, MDPrincipal InvestigatorNew York Langone Health
3 Previous Clinical Trials
285 Total Patients Enrolled
Michael Alaia, MDPrincipal InvestigatorNew York Langone Health
3 Previous Clinical Trials
268 Total Patients Enrolled
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