Design and Rationale for a Randomized, Open-Label, Parallel Clinical Trial Evaluating Major Cardiovascular Events (Pharmacological Treatment Versus Diet Control) in Patients with High-Normal Blood Pressure: The PRINT-TAHA9 Trial

Author:

Attar Armin1ORCID,Mirhosseini Seyed Alireza1,Borazjani Roham1,Sayadi Mehrab1,Ahadi Mahsa1,Zibaeenezhad MohammadJavad1,Razeghian-Jahromi Iman1,Parsa Nader1

Affiliation:

1. Shiraz University of Medical Sciences

Abstract

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 cardiovascular events (MACE). Methods: The PRINT-TAHA9 trial, which is a unicentric, randomized, open-label, placebo-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 allocated 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 six months over a three-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. The study's design adheres to the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidelines. Discussion: The literature on managing high-normal blood pressure reveals a significant gap in medical understanding, especially regarding when to start pharmacological intervention. Despite guidelines advocating early treatment, the debate continues due to insufficient evidence that such interventions significantly reduce major cardiovascular events. 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

Publisher

Springer Science and Business Media LLC

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