- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04153643
Meniscus Surgery Registry
November 18, 2025 updated by: Leslie Bisson, State University of New York at Buffalo
Arthroscopic Partial Meniscectomy Registry
The purpose of this study is to create a data registry of arthroscopic partial meniscectomies performed at our institution.
This information will then be used to examine trends over time, predictive factors, and outcomes of arthroscopic partial meniscectomy.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
376
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Amherst, New York, United States, 14226
- UBMD Orthopaedics & Sports Medicine
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Adults undergoing arthroscopic partial meniscectomy
Description
Inclusion Criteria:
- Scheduled to undergo arthroscopic partial meniscectomy with one of the study investigators at University at Buffalo Medical Doctors Orthopaedics and Sports Medicine
Exclusion Criteria:
- Non-english speaking
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Pain Score
Time Frame: 20 years
|
minimum of 0 (poor function), maximum of 100 (excellent function)
|
20 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 15, 2019
Primary Completion (Actual)
October 28, 2025
Study Completion (Actual)
October 28, 2025
Study Registration Dates
First Submitted
November 1, 2019
First Submitted That Met QC Criteria
November 4, 2019
First Posted (Actual)
November 6, 2019
Study Record Updates
Last Update Posted (Estimated)
November 21, 2025
Last Update Submitted That Met QC Criteria
November 18, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- STUDY00003999
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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