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Clinical Trial Summary

A double-blind, randomized controlled trial designed to evaluate the symptomatic modulating efficacy of amniotic suspension allograft (ASA) in comparison to platelet-rich plasma (PRP), hyaluronic acid (HA) and normal saline (NS) in the injection treatment of knee osteoarthritis. The hypothesis is that ASA would provide the greatest functional improvement.


Clinical Trial Description

At least 150 subjects with osteoarthritic knee will be recruited and computer randomized 1:1:1:1 to single injection of ASA (40mg), ASA (20mg), PRP + HA, and NS groups. Both subjects and evaluaters were blinded to allocations. Functional and radiologic outcomes were measured at baseline, and 1 week, 1, 3, 6, 12 months postinjection. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04698265
Study type Interventional
Source Kaohsiung Veterans General Hospital.
Contact Kuan-Yu Lin
Phone +886-7-3422121
Email johnkyl@yahoo.com
Status Not yet recruiting
Phase N/A
Start date January 1, 2021
Completion date January 31, 2023

See also
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