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Clinical Trial Summary

This randomized clinical trial aims to evaluate the efficacy of liquid platelet-rich fibrin administration at different Wilkes stages.


Clinical Trial Description

Thirty six patients with unilateral painful internal derangement (ID) (Wilkes' 3-4-5) were included. Patients were divided into 2 groups. In group 1 were treated with only artrosythesis. In group 2 were treated with artrosythesis and liquid platelet rich fibrin. In group 2, patients were injected with 1.5-2cc of liquid platelet-rich fibrin within the superior joint space at operation day. Pain and subjective dysfunction were recorded using a visual analog scale and Helkimo index at operation day and tenth day, one month later and 3 months later. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04317560
Study type Interventional
Source Aydin Adnan Menderes University
Contact Burcu GURSOYTRAK
Phone +902562133939
Email dt_burcupoyraz@hotmail.com
Status Recruiting
Phase N/A
Start date March 1, 2019
Completion date April 1, 2020

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