| Literature DB >> 33732434 |
Mauricio Fernandes1, Magdalena Schelotto2, Philipp Maximilian Doldi1,3, Giovanna Milani4, Abul Andrés Ariza Manzano5, Doriam Perera Valdivia6, Alexandra Marie Winter Matos7, Yasmin Hamdy Abdelrahim8, Shaza Ahmed Hamad Bek9, Benito K Benitez10, Vanessa Luiza Romanelli Tavares11, Abdulrahim M Basendwah12, Luis Henrique Albuquerque Sousa13, Naiara Faria Xavier14, Tania Zertuche Maldonado15, Sarah Toyomi de Oliveira16, Melisa Chaker17, Michelle Menon Miyake18, Elif Uygur Kucukseymen19, Kinza Waqar20, Ola M J Alkhozondar21, Ricardo Bernardo da Silva22, Guilhermo Droppelmann23, Antonio Vaz de Macedo24, Rui Nakamura24, Felipe Fregni24.
Abstract
Background: Cancer is the second leading cause of death globally. Up to 86% of advanced cancer patients experience significant pain, while 10-20% live in chronic pain. Besides, increasing prescription of opioids resulted in 33,000 deaths in the US in 2015. Both reduce patients' functional status and quality of life. While cancer survival rates are increasing, therapeutic options for chronic opioid refractory pain are still limited. Esketamine is the s-enantiomer of ketamine, with superior analgesic effect and less psychotomimetic side effects. Intranasal esketamine was approved by the FDA for treatment-resistant depression. However, its use in chronic cancer pain has never been tested. Therefore, we propose a phase II, randomized, placebo-controlled trial to evaluate the efficacy and safety of intranasal esketamine in chronic opioid refractory cancer pain. Methods and analysis: We will recruit 120 subjects with chronic opioid refractory pain, defined as pain lasting more than 3 months despite optimal therapy with high dose opioids (>60 mg morphine equivalent dose/day) and optimal adjuvant therapy. Subjects will be randomized into two groups: intranasal esketamine (56mg) and placebo. Treatment will be administered twice a week for four consecutive weeks. The primary outcome is defined as reduction in the Numeric Pain Rating Scale (NPRS) after first application. Secondary outcomes include NPRS reduction after four weeks, the number of daily morphine rescue doses, functional status and satisfaction, and depression.Entities:
Keywords: Cancer pain; Esketamine; Opioid refractory; Pain measurement
Year: 2021 PMID: 33732434 PMCID: PMC7885290 DOI: 10.12688/f1000research.27809.1
Source DB: PubMed Journal: F1000Res ISSN: 2046-1402