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Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study

INTRODUCTION: Currently available treatments for chronic lower back pain (CLBP) do not adequately address both nociceptive and neuropathic components of pain. We evaluated efficacy and safety of fixed-dose combination (FDC) of low-dose pregabalin prolonged release 75 mg–etoricoxib 60 mg to address b...

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Autores principales: Yeole, Amit B., Sree Ranga Lakshmi, G., Selvakumar, C. J., Goni, Vijay G., Nawal, C. L., Valya, Bhanoth J., Patel, Brijesh J., Patel, Rohit D., Pawar, Eknath D., Panigrahi, Ranajit, Kumar, Ashish Y., Shintre, Shrinivas S., Devkare, Prashant H., Dharmadhikari, Shruti K., Choudhari, Sanjay Y., Doshi, Maulik S., Mehta, Suyog C., Joglekar, Sadhna J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633919/
https://www.ncbi.nlm.nih.gov/pubmed/36224489
http://dx.doi.org/10.1007/s40122-022-00437-2
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author Yeole, Amit B.
Sree Ranga Lakshmi, G.
Selvakumar, C. J.
Goni, Vijay G.
Nawal, C. L.
Valya, Bhanoth J.
Patel, Brijesh J.
Patel, Rohit D.
Pawar, Eknath D.
Panigrahi, Ranajit
Kumar, Ashish Y.
Shintre, Shrinivas S.
Devkare, Prashant H.
Dharmadhikari, Shruti K.
Choudhari, Sanjay Y.
Doshi, Maulik S.
Mehta, Suyog C.
Joglekar, Sadhna J.
author_facet Yeole, Amit B.
Sree Ranga Lakshmi, G.
Selvakumar, C. J.
Goni, Vijay G.
Nawal, C. L.
Valya, Bhanoth J.
Patel, Brijesh J.
Patel, Rohit D.
Pawar, Eknath D.
Panigrahi, Ranajit
Kumar, Ashish Y.
Shintre, Shrinivas S.
Devkare, Prashant H.
Dharmadhikari, Shruti K.
Choudhari, Sanjay Y.
Doshi, Maulik S.
Mehta, Suyog C.
Joglekar, Sadhna J.
author_sort Yeole, Amit B.
collection PubMed
description INTRODUCTION: Currently available treatments for chronic lower back pain (CLBP) do not adequately address both nociceptive and neuropathic components of pain. We evaluated efficacy and safety of fixed-dose combination (FDC) of low-dose pregabalin prolonged release 75 mg–etoricoxib 60 mg to address both pain components. METHODS: This randomized phase 3 trial conducted at 12 centres across India evaluated efficacy (based on mean change in numeric rating scale [NRS], Roland–Morris disability questionnaire [RDQ], visual analogue scale [VAS], patient global impression of improvement [PGI-I], clinical global impression of improvement [CGI-I] and rescue medication consumption) and safety of FDC in comparison to etoricoxib alone in adult patients with CLBP. Treatment duration was 8 weeks. RESULTS: Of the 371 patients screened, 319 were randomized and considered for efficacy and safety analysis. Both treatment groups had no significant difference in terms of demography and baseline disease characteristics. Significantly better outcomes with FDC compared to etoricoxib were observed at week 4 onwards. At week 8, both groups showed significant reduction in mean NRS score from baseline (− 4.00 ± 1.65 in FDC; − 2.92 ± 1.59 in etoricoxib) with mean NRS score being significantly less in the FDC group compared to etoricoxib group (3.26 ± 1.56 vs 4.31 ± 1.56; p < 0.0001). The FDC was more effective than etoricoxib in terms of significantly greater reduction in RDQ score (− 9.28 ± 4.48 vs − 6.78 ± 4.34; p < 0.0001) and VAS score (− 37.66 ± 18.7 vs − 28.50 ± 16.31; p < 0.0001) at week 8. The FDC was also better in terms of significantly more patients reporting their condition as ‘very much better’ (36.9% vs 5.0%; p < 0.0001) and clinicians reporting patient’s condition as ‘very much improved’ (36.3% vs 5.7%; p < 0.0001). Overall, study medications were well tolerated. CONCLUSION: FDC of pregabalin and etoricoxib provided significant benefits in reducing pain and improving functional status compared with etoricoxib alone in patients with CLBP. Pregabalin prolonged release–etoricoxib FDC could be one of the treatment options for early and sustained pain relief and improvement in quality-of-life in treating CLBP as it addresses both neuropathic and nociceptive components of pain. TRIAL REGISTRATION: CTRI/2018/10/015886. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40122-022-00437-2.
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spelling pubmed-96339192022-12-07 Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study Yeole, Amit B. Sree Ranga Lakshmi, G. Selvakumar, C. J. Goni, Vijay G. Nawal, C. L. Valya, Bhanoth J. Patel, Brijesh J. Patel, Rohit D. Pawar, Eknath D. Panigrahi, Ranajit Kumar, Ashish Y. Shintre, Shrinivas S. Devkare, Prashant H. Dharmadhikari, Shruti K. Choudhari, Sanjay Y. Doshi, Maulik S. Mehta, Suyog C. Joglekar, Sadhna J. Pain Ther Original Research INTRODUCTION: Currently available treatments for chronic lower back pain (CLBP) do not adequately address both nociceptive and neuropathic components of pain. We evaluated efficacy and safety of fixed-dose combination (FDC) of low-dose pregabalin prolonged release 75 mg–etoricoxib 60 mg to address both pain components. METHODS: This randomized phase 3 trial conducted at 12 centres across India evaluated efficacy (based on mean change in numeric rating scale [NRS], Roland–Morris disability questionnaire [RDQ], visual analogue scale [VAS], patient global impression of improvement [PGI-I], clinical global impression of improvement [CGI-I] and rescue medication consumption) and safety of FDC in comparison to etoricoxib alone in adult patients with CLBP. Treatment duration was 8 weeks. RESULTS: Of the 371 patients screened, 319 were randomized and considered for efficacy and safety analysis. Both treatment groups had no significant difference in terms of demography and baseline disease characteristics. Significantly better outcomes with FDC compared to etoricoxib were observed at week 4 onwards. At week 8, both groups showed significant reduction in mean NRS score from baseline (− 4.00 ± 1.65 in FDC; − 2.92 ± 1.59 in etoricoxib) with mean NRS score being significantly less in the FDC group compared to etoricoxib group (3.26 ± 1.56 vs 4.31 ± 1.56; p < 0.0001). The FDC was more effective than etoricoxib in terms of significantly greater reduction in RDQ score (− 9.28 ± 4.48 vs − 6.78 ± 4.34; p < 0.0001) and VAS score (− 37.66 ± 18.7 vs − 28.50 ± 16.31; p < 0.0001) at week 8. The FDC was also better in terms of significantly more patients reporting their condition as ‘very much better’ (36.9% vs 5.0%; p < 0.0001) and clinicians reporting patient’s condition as ‘very much improved’ (36.3% vs 5.7%; p < 0.0001). Overall, study medications were well tolerated. CONCLUSION: FDC of pregabalin and etoricoxib provided significant benefits in reducing pain and improving functional status compared with etoricoxib alone in patients with CLBP. Pregabalin prolonged release–etoricoxib FDC could be one of the treatment options for early and sustained pain relief and improvement in quality-of-life in treating CLBP as it addresses both neuropathic and nociceptive components of pain. TRIAL REGISTRATION: CTRI/2018/10/015886. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40122-022-00437-2. Springer Healthcare 2022-10-12 2022-12 /pmc/articles/PMC9633919/ /pubmed/36224489 http://dx.doi.org/10.1007/s40122-022-00437-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Yeole, Amit B.
Sree Ranga Lakshmi, G.
Selvakumar, C. J.
Goni, Vijay G.
Nawal, C. L.
Valya, Bhanoth J.
Patel, Brijesh J.
Patel, Rohit D.
Pawar, Eknath D.
Panigrahi, Ranajit
Kumar, Ashish Y.
Shintre, Shrinivas S.
Devkare, Prashant H.
Dharmadhikari, Shruti K.
Choudhari, Sanjay Y.
Doshi, Maulik S.
Mehta, Suyog C.
Joglekar, Sadhna J.
Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title_full Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title_fullStr Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title_full_unstemmed Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title_short Efficacy and Safety of Pregabalin Prolonged Release–Etoricoxib Combination Compared to Etoricoxib for Chronic Low Back Pain: Phase 3, Randomized Study
title_sort efficacy and safety of pregabalin prolonged release–etoricoxib combination compared to etoricoxib for chronic low back pain: phase 3, randomized study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9633919/
https://www.ncbi.nlm.nih.gov/pubmed/36224489
http://dx.doi.org/10.1007/s40122-022-00437-2
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