Prospective Registry of Anterior Cruciate Ligament Reconstructions

Sponsor
State University of New York at Buffalo (Other)
Overall Status
Recruiting
CT.gov ID
NCT04135950
Collaborator
(none)
900
1
552
1.6

Study Details

Study Description

Brief Summary

The purpose of the study is to investigate factors that are associated with outcomes of injury to the anterior cruciate ligament (ACL) in the knee among patients who are undergoing surgical reconstruction. This study is a registry of all patients having knee surgery at our institution performed by 4 fellowship-trained orthopaedic surgeons. The surgeon documents patient information on standard data forms including risk factors and surgical findings.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    900 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Prospective Registry of Predictors and Comorbid Injuries Associated With Anterior Cruciate Ligament Reconstructions
    Actual Study Start Date :
    Jan 1, 2005
    Anticipated Primary Completion Date :
    Jan 1, 2050
    Anticipated Study Completion Date :
    Jan 1, 2051

    Outcome Measures

    Primary Outcome Measures

    1. additional injury [intraoperatively]

      At the time of ACL surgery, it is determined if the patient has any other injuries to the meniscus or cartilage.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients undergoing ACL surgery
    Exclusion Criteria:
    • Previous surgery on the affected knee

    • Posterior cruciate ligament injuries

    • Grade 2 lateral collateral ligament or medial collateral ligament injuries

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UBMD Orthopaedics and Sports Medicine Buffalo New York United States 14226

    Sponsors and Collaborators

    • State University of New York at Buffalo

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Leslie Bisson, June A. and Eugene R. Mindell, MD Professor and Chair, State University of New York at Buffalo
    ClinicalTrials.gov Identifier:
    NCT04135950
    Other Study ID Numbers:
    • 441874-2
    First Posted:
    Oct 23, 2019
    Last Update Posted:
    May 17, 2022
    Last Verified:
    May 1, 2022
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 17, 2022