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Clinical and translational science · 2024

Implementing a pragmatic clinical trial to tailor opioids for chronic pain on behalf of the IGNITE ADOPT PGx investigators.

Протокол клинического исследованияСтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Skaar Todd C, Myers Rachel A, Fillingim Roger B, Callaghan John T, Cicali Emily, Eadon Michael T, Elwood Erica N, Ginsburg Geoffrey S, Lynch Sheryl, Nguyen Khoa A, Obeng Aniwaa Owusu, Park Haesuk, Pratt Victoria M, Rosenman Marc, Sadeghpour Azita, Shuman Saskia, Singh Rajbir, Tillman Emma M, Volpi Simona, Wiisanen Kristin, Winterstein Almut G, Horowitz Carol R, Voora Deepak, Orlando Lori, Chakraborty Hrishikesh, Van Driest Sara, Peterson Josh F, Cavallari Larisa A, Johnson Julie A, Dexter Paul R, IGNITE Pragmatic Trials Network

Аннотация

Chronic pain is a prevalent condition with enormous economic burden. Opioids such as tramadol, codeine, and hydrocodone are commonly used to treat chronic pain; these drugs are activated to more potent opioid receptor agonists by the hepatic CYP2D6 enzyme. Results from clinical studies and mechanistic understandings suggest that CYP2D6-guided therapy will improve pain control and reduce adverse drug events. However, CYP2D6 is rarely used in clinical practice due in part to the demand for additional clinical trial evidence. Thus, we designed the ADOPT-PGx (A Depression and Opioid Pragmatic Trial in Pharmacogenetics) chronic pain study, a multicenter, pragmatic, randomized controlled clinical trial, to assess the effect of CYP2D6 testing on pain management. The study enrolled 1048 participants who are taking or being considered for treatment with CYP2D6-impacted opioids for their chronic pain. Participants were randomized to receive immediate or delayed (by 6 months) genotyping of CYP2D6 with clinical decision support (CDS). CDS encouraged the providers to follow the CYP2D6-guided trial recommendations. The primary study outcome is the 3-month absolute change in the composite pain intensity score assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) measures. Follow-up will be completed in July 2024. Herein, we describe the design of this trial along with challenges encountered during enrollment.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты