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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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Detalles Bibliográficos
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
Descripción
Sumario: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.