Effectiveness of Oral Hyaluronic Acid in Knee Osteoarthritis

Status Completed

Clinical Trial Summary

This study was a randomized, double-blind, placebo-controlled study evaluating the efficacy of an oral liquid HA supplement (A+HA) in symptoms relief and improvement of quality of life in knee osteoarthritis patients with mild knee pain.

Clinical Trial Description

Subjects were initially screened at the Randomization/Baseline Visit (Week 0). Eligible subjects were randomized at the same visit into the treatment period and received the assigned treatment in a double-blind fashion for 8 weeks. During the 8 weeks treatment period, there were three follow-up visits requested (Week 2, Week 4 and Week 8). Efficacy was measured by using Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the Short Form-36 (SF-36). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04352322
Study type	Interventional
Source	China Medical University Hospital
Contact
Status	Completed
Phase	N/A
Start date	January 2012
Completion date	July 2016

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