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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04135950
Other study ID # 441874-2
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2005
Est. completion date January 2051

Study information

Verified date July 2023
Source State University of New York at Buffalo
Contact Nomi S Weiss-Laxer, PhD
Phone 716-881-8904
Email nomiweis@buffalo.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 900
Est. completion date January 2051
Est. primary completion date January 2050
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UBMD Orthopaedics and Sports Medicine Buffalo New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary additional injury At the time of ACL surgery, it is determined if the patient has any other injuries to the meniscus or cartilage. intraoperatively
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