دورية أكاديمية

The coArtHA trial—identifying the most effective treatment strategies to control arterial hypertension in sub-Saharan Africa: study protocol for a randomized controlled trial

التفاصيل البيبلوغرافية
العنوان: The coArtHA trial—identifying the most effective treatment strategies to control arterial hypertension in sub-Saharan Africa: study protocol for a randomized controlled trial
المؤلفون: Mapesi, Herry, Gupta, Ravi, Wilson, Herieth Ismael, Lukau, Blaise, Amstutz, Alain, Lyimo, Aza, Muhairwe, Josephine, Senkoro, Elizabeth, Byakuzana, Theonestina, Mphunyane, Madavida, Bresser, Moniek, Glass, Tracy Renée, Lambiris, Mark, Fink, Günther, Gingo, Winfrid, Battegay, Manuel, Paris, Daniel Henry, Rohacek, Martin, Vanobberghen, Fiona, Labhardt, Niklaus Daniel, Burkard, Thilo, Weisser, Maja
المساهمون: Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
المصدر: Trials ; volume 22, issue 1 ; ISSN 1745-6215
بيانات النشر: Springer Science and Business Media LLC
سنة النشر: 2021
مصطلحات موضوعية: Pharmacology (medical), Medicine (miscellaneous)
الوصف: Background Arterial hypertension is the most prevalent risk factor for cardiovascular disease in sub-Saharan Africa. Only a few and mostly small randomized trials have studied antihypertensive treatments in people of African descent living in sub-Saharan Africa. Methods In this open-label, three-arm, parallel randomized controlled trial conducted at two rural hospitals in Lesotho and Tanzania, we compare the efficacy and cost-effectiveness of three antihypertensive treatment strategies among participants aged ≥ 18 years. The study includes patients with untreated uncomplicated arterial hypertension diagnosed by a standardized office blood pressure ≥ 140/90 mmHg. The trial encompasses a superiority comparison between a triple low-dose antihypertensive drug combination versus the current standard of care (monotherapy followed by dual treatment), as well as a non-inferiority comparison for a dual drug combination versus standard of care with optional dose titration after 4 and 8 weeks for participants not reaching the target blood pressure. The sample size is 1268 participants with parallel allocation and a randomization ratio of 2:1:2 for the dual, triple and control arms, respectively. The primary endpoint is the proportion of participants reaching a target blood pressure at 12 weeks of ≤ 130/80 mmHg and ≤ 140/90 mmHg among those aged < 65 years and ≥ 65 years, respectively. Clinical manifestations of end-organ damage and cost-effectiveness at 6 months are secondary endpoints. Discussion This trial will help to identify the most effective and cost-effective treatment strategies for uncomplicated arterial hypertension among people of African descent living in rural sub-Saharan Africa and inform future clinical guidelines on antihypertensive management in the region. Trial registration Clinicaltrials.gov NCT04129840 . Registered on 17 October 2019 ( https://www.clinicaltrials.govTest/ ).
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1186/s13063-021-05023-z
DOI: 10.1186/s13063-021-05023-z.pdf
DOI: 10.1186/s13063-021-05023-z/fulltext.html
الإتاحة: https://doi.org/10.1186/s13063-021-05023-zTest
حقوق: http://creativecommons.org/licenses/by/4.0Test/ ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.A7066790
قاعدة البيانات: BASE