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NCT05735899

Evaluation of the Safety and Efficacy of Meniscal Preservation Surgery

Status unknown Last updated 21 February 2024
What this trial tests

trial in Meniscal Extrusion in 20 participants. Status unknown.

Timeline
16 August 2022
Primary endpoint
16 August 2025
16 August 2025

Quick facts

Lead sponsorAndrews Research & Education Foundation
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment20
Start date16 August 2022
Primary completion16 August 2025
Estimated completion16 August 2025
Sites1 location across United States

Conditions studied

Sponsor

Andrews Research & Education Foundation

Who can join

18 and older, any sex, with Meniscal Extrusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The primary objective of this study is to demonstrate the safety and efficacy of surgical meniscal preservation techniques to correct meniscal extrusion. The primary endpoint for safety will be analysis of the total number and types of adverse events (AEs) and serious adverse events (SAEs). The primary endpoint for efficacy will include analysis of patient report outcome measures (PROMs). H0 - Participants undergoing surgical meniscal preservation to correct meniscal extrusion will not exhibit a limited number of safety events nor have favorable outcomes. H1- Participants undergoing surgical meniscal preservation to correct meniscal extrusion will exhibit a limited number of safety events and have favorable outcomes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Meniscal Extrusion

Currently open trials in the same condition.

Other Andrews Research & Education Foundation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05735899.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing