Design and rationale for a randomized, open-label, parallel clinical trial evaluating major adverse cardiovascular events (pharmacological treatment versus diet control) in patients with high-normal blood pressure: the PRINT-TAHA9 trial.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Trials Pub Date : 2024-08-26 DOI:10.1186/s13063-024-08420-2
Armin Attar, Seyed Alireza Mirhosseini, Roham Borazjani, Mehrab Sayadi, Mahsa Ahadi, MohammadJavad Zibaeenezhad, Iman Razeghian-Jahromi, Nader Parsa
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Abstract

Background: The distinction between normal and high blood pressure remains a debated topic, with varying guidelines on when to start medication. Contemporary guidelines advocate for the initiation of antihypertensive therapy in individuals who present with high-normal blood pressure, particularly those exhibiting elevated 10-year atherosclerotic cardiovascular disease (ASCVD) risk scores. Despite these recommendations, there is a notable lack of direct evidence supporting the efficacy of treating high-normal blood pressure to prevent major adverse cardiovascular events (MACE).

Methods: The PRINT-TAHA9 trial, a unicentric, randomized, open-label, controlled, parallel clinical study, seeks to explore the effects of intensive blood pressure control on MACE in participants with high-normal blood pressure. We will enroll 1620 adults aged 18 years and above with a systolic blood pressure range of 130-140 mmHg, diastolic blood pressure under 90 mmHg, and atherosclerotic cardiovascular disease (ASCVD) risk score exceeding 7.5%. The study will be executed in five distinct phases, with each phase enrolling between 300 and 400 participants. Participants will be randomly assigned to either the treatment group receiving antihypertensive medication (amlodipine/valsartan) and a low-salt/low-fat diet or to the control group receiving a similar diet. Follow-up visits are scheduled every 6 months over a 3-year period to monitor blood pressure, evaluate medication adherence, document any adverse events, and adjust the intervention as necessary. Cox proportional hazards regression analysis will be employed to examine the disparities between the two arms.

Discussion: Despite guidelines promoting early treatment of elevated blood pressure, the debate continues due to insufficient evidence that such interventions significantly reduce the occurrence of MACE. This trial seeks to address this critical evidence gap.

Trial registration: The PRINT-TAHA9 trial was registered in October 2019 with the Iranian Registry of Clinical Trials (IRCT.ir) under the registration number IRCT20191002044961N1. https://irct.behdasht.gov.ir/trial/43092 .

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评估高血压正常值患者主要心血管不良事件(药物治疗与饮食控制)的随机、开放标签、平行临床试验的设计与原理:PRINT-TAHA9 试验。
背景:血压正常与血压高之间的区别仍是一个备受争议的话题,关于何时开始用药的指南也各不相同。当代指南主张对血压正常者,尤其是 10 年动脉粥样硬化性心血管疾病(ASCVD)风险评分升高者,开始降压治疗。尽管有这些建议,但明显缺乏直接证据支持高血压治疗对预防重大不良心血管事件(MACE)的疗效:PRINT-TAHA9试验是一项单中心、随机、开放标签、对照、平行临床研究,旨在探索强化血压控制对高血压患者MACE的影响。我们将招募 1620 名年龄在 18 岁及以上、收缩压在 130-140 mmHg 之间、舒张压在 90 mmHg 以下、动脉粥样硬化性心血管疾病(ASCVD)风险评分超过 7.5%的成年人。该研究将分五个不同阶段进行,每个阶段将招募 300 到 400 名参与者。参与者将被随机分配到接受降压药物(氨氯地平/缬沙坦)和低盐/低脂饮食的治疗组或接受类似饮食的对照组。在为期 3 年的时间里,每 6 个月进行一次随访,以监测血压、评估服药依从性、记录任何不良事件,并在必要时调整干预措施。我们将采用 Cox 比例危险回归分析来研究两组之间的差异:讨论:尽管指南提倡尽早治疗血压升高,但由于没有足够证据表明这种干预措施能显著减少 MACE 的发生,因此争论仍在继续。本试验旨在填补这一关键证据缺口:PRINT-TAHA9 试验于 2019 年 10 月在伊朗临床试验注册中心(IRCT.ir)注册,注册号为 IRCT20191002044961N1。https://irct.behdasht.gov.ir/trial/43092 。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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