ESCAPE pain trial - The effects of Curcumin in pain relief in women diagnosed with primary dysmenorrhea: A triple blinded, placebo-controlled, phase II, randomized clinical trial protocol.

Main Article Content

Elly Pichardo, MD.
Tatiana Liborio-Kimura, DDS, PhD.
Maria del Pilar Estrella Caballero
Vahid Nouri Kandany, MD
Lucas Augusto Pepe Mena
Edson Santos Ferreira Filho, MD.
Eduardo Dytz Almeida, MD, MSc.
Ana Isabel Sanchez-Barbero, MD.
Susan Benedict Navia
Alberto Durán-Peña, MD.
Khalid Ali S S Al-Karbi, MD.
Marianne Zelniker, MD.
Diego Greatti Vaz da Silva, MD.
Mariane Schäffer Castro
Cassiano Ricardo de Oliveira Berto
Clarissa Medeiros, MD.
Danielli Matsuura, MD.
Daniel Eduardo Carvajal-Hausdorf, MD.
Carlos Augusto Rossetti
Camelia Tang Qian Ying, MD.
Bruno Soares Rocha Calabria, MD.
Gustavo de Almeida, MD.
Kamran Mushtaq
Ana Luisa Soares Neves, MD
Gustavo Costa Nascimento de Carvalho
Ahmed Abdallah Ahmed Abdallah
Ahmed Doomi, MBBS, CABNS, FEBNS, FRCS
Matteo Guidetti
Eladio Radhames Perez Antonio
Sachin Thakuji Thigale
Pedro Oliveira, DDM, MD, PhD.
Arturo Tamayo, MD, FAHA, MSc.
Denise Saretta Schwartz, DVM, MSc, PhD.

Abstract

Introduction: Primary dysmenorrhea affects many women, being a major cause of absenteeism and reduced productivity at work and at school. Although non-steroidal anti-inflammatory drugs (NSAIDs) are a good treatment option, up to 18% of women show no response or present allergic reactions and adverse events. Curcumin has antispasmodic, antinociceptive, and both specific and nonspecific anti-inflammatory effects, with good tolerability and safety. To date, no previous trial involving curcumin and dysmenorrhea pain has been performed. Therefore, our main goal is to assess the efficacy of curcumin for pain relief among women with primary dysmenorrhea, along with determining curcumin’s adverse effects and tolerability profile.
Methods: A phase II, single-center, randomized, triple-blinded, placebo-controlled, parallel-group, superiority trial to evaluate the effect of curcumin (500 mg/12h) in pain reduction in women (18 to 35-year-old) with primary dysmenorrhea. A first cycle will be used for a passive, observational run-in phase. A sample of 108 participants (54 per group) is necessary to detect a 30% difference in pain sensitivity between groups assessed by visual analogue scale (VAS). Secondary outcomes include side effects, Cox Menstrual Symptom Scale (CMSS), and use of rescue drugs for pain relief.
Discussion: Clinical evidence has shown analgesic and anti-inflammatory effects of curcumin and in view of dysmenorrhea’s physiopathology being related to those mechanisms targeted by curcumin, we hypothesize its use could represent an innovative and effective therapy to reduce the severity of this disease and its symptoms.


Keywords: primary dysmenorrhea, Curcumin, pain relief, Visual Analogue Scale, Cox Menstrual Symptom Scale.

Article Details

How to Cite
ESCAPE pain trial - The effects of Curcumin in pain relief in women diagnosed with primary dysmenorrhea: A triple blinded, placebo-controlled, phase II, randomized clinical trial protocol. (2020). Principles and Practice of Clinical Research, 6(2). https://doi.org/10.21801/ppcrj.2020.62.5
Section
Clinical Research Design

How to Cite

ESCAPE pain trial - The effects of Curcumin in pain relief in women diagnosed with primary dysmenorrhea: A triple blinded, placebo-controlled, phase II, randomized clinical trial protocol. (2020). Principles and Practice of Clinical Research, 6(2). https://doi.org/10.21801/ppcrj.2020.62.5

Most read articles by the same author(s)