An open label, prospective, clinical study on a polyherbal formulation in osteoarthritis of knee

Autor: Sanjay U Nipanikar; Manjit Saluja; Vinod V Kuber; Kalyan P Kadbhane; Arvind Chopra; Namdev R Khade
Sprache: Englisch
Veröffentlicht: 2013
Quelle: Directory of Open Access Journals: DOAJ Articles
Online Zugang: http://www.jaim.in/article.asp?issn=0975-9476;year=2013;volume=4;issue=1;spage=33;epage=39;aulast=Nipanikar
https://doaj.org/toc/0975-9476
0975-9476
doi:10.4103/0975-9476.109549
https://doaj.org/article/6cc930f8046b4e5cacf01cc23ba43d7e
https://doi.org/10.4103/0975-9476.109549
https://doaj.org/article/6cc930f8046b4e5cacf01cc23ba43d7e
Erfassungsnummer: ftdoajarticles:oai:doaj.org/article:6cc930f8046b4e5cacf01cc23ba43d7e

Zusammenfassung

Background: Currently, though pharmacological, mechanical, and surgical interventions are used, there is no known cure for osteoarthritis (OA). Objectives: The main aim of the study was to assess the efficacy and safety of "TLPL/AY/03/2008," a polyherbal formulation on knee joint pain assessed on visual analogue scale (VAS) and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Materials and Methods: It was an open label, single center, prospective, clinical study conducted in 36 patients of OA Knee. Two capsules of ′TLPL/AY/03/2008′ were given to all patients twice daily orally after meals for 180 days. Results: Data describing quantitative measures are expressed as mean ± SD. Comparison of variables representing categorical data was performed using Chi-square test. The mean joint pain (as assessed on VAS) reduced significantly (59.85%; P < 0.05) and the mean WOMAC combined score, WOMAC pain sub-score, WOMAC stiffness sub-score, and WOMAC difficulty sub-score also reduced significantly at the end of the study. The mean time taken by the patients to walk 50 feet too, was reduced significantly (25.26%) at the end of the study. At the end of 4 months of the treatment, no patient needed paracetamol as rescue medicine to control pain. Most of the patients had shown good overall improvement assessed by the physician and by the patients. Majority of the patients showed excellent tolerability to the study drug. No significant change in most of the safety laboratory parameters was observed at the end of the study. Conclusion: The study provides good evidence in support of the efficacy and safety of the ′TLPL/AY/03/2008′ in OA of knee.