Cargando…
A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial
OBJECTIVES: The aim of the study was to demonstrate the non-inferiority of a single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate (SH) vs 0.8% hylan G-F 20 (control) in symptomatic knee osteoarthritis. DESIGN: This was a double-blind, randomized, controlled trial condu...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903764/ https://www.ncbi.nlm.nih.gov/pubmed/31821355 http://dx.doi.org/10.1371/journal.pone.0226007 |
_version_ | 1783477907604111360 |
---|---|
author | Maheu, Emmanuel Avouac, Bernard Dreiser, Renée Liliane Bardin, Thomas |
author_facet | Maheu, Emmanuel Avouac, Bernard Dreiser, Renée Liliane Bardin, Thomas |
author_sort | Maheu, Emmanuel |
collection | PubMed |
description | OBJECTIVES: The aim of the study was to demonstrate the non-inferiority of a single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate (SH) vs 0.8% hylan G-F 20 (control) in symptomatic knee osteoarthritis. DESIGN: This was a double-blind, randomized, controlled trial conducted in patients with painful tibiofemoral osteoarthritis (American College of Rheumatology criteria) with insufficient response or intolerance to first-line analgesics and regular non-steroidal anti-inflammatory drugs. Subjects received a single intra-articular injection of either SH or hylan G-F 20. The primary outcome was the 6-month change from baseline in the Western Ontario and McMaster Universities Osteoarthritis Index pain subscale (WOMAC A), with a pre-specified lower margin for non-inferiority of 8 mm. RESULTS: Of the 292 patients randomized (SH: 144), 288 received an injection (SH: 142), 266 completed the study (SH: 134). In the Per Protocol dataset (SH: 113, control: 112), the WOMAC A change at 6 months was -34.3 mm (95% confidence interval (CI): -37.8, -30.8) and -36.2 mm (95% CI: -40.3, -32.1) for the SH and hylan G-F 20 patients, respectively (P = 0.5). The intergroup difference was -1.9 mm (95% CI: -7.3, 3.5). Results were similar in the Full Analysis Set (SH: 139, control: 141) with a difference between the groups of -2.9 mm (95% CI: -7.9, 2.2). A total of 31.3% of the injected patients reported a treatment-emergent adverse event, including injection site reactions (pain, inflammation or effusion) which occurred in 8.5% of the SH patients vs 13.0% of the hylan G-F 20 patients. No serious reactions were reported. CONCLUSIONS: This clinical trial demonstrated the non-inferiority of a single intra-articular injection of SH vs hylan G-F 20 on the WOMAC A change from baseline at 6 months. |
format | Online Article Text |
id | pubmed-6903764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69037642019-12-20 A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial Maheu, Emmanuel Avouac, Bernard Dreiser, Renée Liliane Bardin, Thomas PLoS One Research Article OBJECTIVES: The aim of the study was to demonstrate the non-inferiority of a single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate (SH) vs 0.8% hylan G-F 20 (control) in symptomatic knee osteoarthritis. DESIGN: This was a double-blind, randomized, controlled trial conducted in patients with painful tibiofemoral osteoarthritis (American College of Rheumatology criteria) with insufficient response or intolerance to first-line analgesics and regular non-steroidal anti-inflammatory drugs. Subjects received a single intra-articular injection of either SH or hylan G-F 20. The primary outcome was the 6-month change from baseline in the Western Ontario and McMaster Universities Osteoarthritis Index pain subscale (WOMAC A), with a pre-specified lower margin for non-inferiority of 8 mm. RESULTS: Of the 292 patients randomized (SH: 144), 288 received an injection (SH: 142), 266 completed the study (SH: 134). In the Per Protocol dataset (SH: 113, control: 112), the WOMAC A change at 6 months was -34.3 mm (95% confidence interval (CI): -37.8, -30.8) and -36.2 mm (95% CI: -40.3, -32.1) for the SH and hylan G-F 20 patients, respectively (P = 0.5). The intergroup difference was -1.9 mm (95% CI: -7.3, 3.5). Results were similar in the Full Analysis Set (SH: 139, control: 141) with a difference between the groups of -2.9 mm (95% CI: -7.9, 2.2). A total of 31.3% of the injected patients reported a treatment-emergent adverse event, including injection site reactions (pain, inflammation or effusion) which occurred in 8.5% of the SH patients vs 13.0% of the hylan G-F 20 patients. No serious reactions were reported. CONCLUSIONS: This clinical trial demonstrated the non-inferiority of a single intra-articular injection of SH vs hylan G-F 20 on the WOMAC A change from baseline at 6 months. Public Library of Science 2019-12-10 /pmc/articles/PMC6903764/ /pubmed/31821355 http://dx.doi.org/10.1371/journal.pone.0226007 Text en © 2019 Maheu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Maheu, Emmanuel Avouac, Bernard Dreiser, Renée Liliane Bardin, Thomas A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title | A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title_full | A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title_fullStr | A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title_full_unstemmed | A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title_short | A single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan G-F 20 in the treatment of symptomatic knee osteoarthritis: A 6-month, multicenter, randomized, controlled non-inferiority trial |
title_sort | single intra-articular injection of 2.0% non-chemically modified sodium hyaluronate vs 0.8% hylan g-f 20 in the treatment of symptomatic knee osteoarthritis: a 6-month, multicenter, randomized, controlled non-inferiority trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903764/ https://www.ncbi.nlm.nih.gov/pubmed/31821355 http://dx.doi.org/10.1371/journal.pone.0226007 |
work_keys_str_mv | AT maheuemmanuel asingleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT avouacbernard asingleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT dreiserreneeliliane asingleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT bardinthomas asingleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT maheuemmanuel singleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT avouacbernard singleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT dreiserreneeliliane singleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial AT bardinthomas singleintraarticularinjectionof20nonchemicallymodifiedsodiumhyaluronatevs08hylangf20inthetreatmentofsymptomatickneeosteoarthritisa6monthmulticenterrandomizedcontrollednoninferioritytrial |