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Comparing duloxetine and pregabalin for treatment of pain and depression in women with fibromyalgia: an open-label randomized clinical trial.
Bidari, Ali; Moazen-Zadeh, Ehsan; Ghavidel-Parsa, Banafsheh; Rahmani, Shahrzad; Hosseini, Sajjad; Hassankhani, Amir.
Afiliação
  • Bidari A; Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.
  • Moazen-Zadeh E; Psychiatric Research Center, Roozbeh Hospital, Tehran University of Medical Sciences, Tehran, Iran.
  • Ghavidel-Parsa B; Institute of Mental Health, Department of Psychiatry, University of British Columbia, Vancouver, Canada.
  • Rahmani S; Rheumatology Research Center, Razi Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran. bghavidelparsa@gmail.com.
  • Hosseini S; Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.
  • Hassankhani A; Department of General Medicine, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
Daru ; 27(1): 149-158, 2019 Jun.
Article em En | MEDLINE | ID: mdl-30877484
ABSTRACT

BACKGROUND:

Duloxetine and pregabalin are among the most widely used medications in the treatment of patients with fibromyalgia syndrome (FM).

OBJECTIVES:

To add to the very few lines of evidence that exist on the comparative safety and efficacy of these two medications.

METHODS:

In this open-label randomized clinical trial, outpatient women, who were diagnosed with FM based on American College of Rheumatology 2010 criteria, and had an age range of 18-65 years old were assigned to either duloxetine 30-60 mg or pregabalin 75-150 mg per day for 4 weeks. Patients were excluded in cases of having used duloxetine, pregabalin, gabapentin, or antidepressants within 12 weeks prior to the study, having had a history of comorbid medical conditions that could provoke chronic pain, or having had comorbid neuropsychiatric disorders, except for major depressive/anxiety disorders. Primary outcomes were between-group differences in mean score changes from baseline to end point for Widespread Pain Index (WPI) and Beck Depression Inventory-II. Secondary outcomes were the same statistical estimates, but for Fibromyalgia Impact Questionnaire-Revised and 12-Item Short Form Survey. Descriptive statistics and independent samples t-test were the main methods of analysis. ( www.irct.ir ; IRCT2016030626935N1).

RESULTS:

Among all the scales, only WPI scores improved with a statistically significant difference between the two treatment arms, favoring duloxetine (Mean difference in score change - 2.32, 95% CI, -4.46 to - 0.18; p = 0.034; Cohen's d 0.53 95% CI, 0.04 to 1.02). Drop out rate and cumulative incidence of nausea was significantly higher in the duloxetine arm compared to the pregabalin arm.

CONCLUSION:

This study provides further evidence on higher efficacy of duloxetine compared to pregabalin for the treatment of pain in patients with fibromyalgia. Future comprehensive pragmatic clinical trials are warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibromialgia / Depressão / Dor Crônica / Pregabalina / Cloridrato de Duloxetina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibromialgia / Depressão / Dor Crônica / Pregabalina / Cloridrato de Duloxetina Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article