← Eichor
Study identifier: NCT03264352 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intervention for High-normal Blood Pressure in Adults With Type 2 Diabetes

Condition: Diabetes Mellitus, Type 2 · Adverse Event · Blood Pressure  ·  Sponsor: XueQing Yu

PhasePhase 4
Planned participants11414
Who can joinAll sexes, 45 Years to 79 Years
Healthy volunteersNo

About this study

Lowering of blood pressure (BP) in high-risk hypertensive individuals reduces major adverse cardiovascular and cerebrovascular events. Diabetic patients with hypertension benefit from BP lowering treatment. The present trial, IPAD in brief, is a randomized, open-label, parallel-designed, multicenter study involving nearly 12,000 patients to be recruited and to be followed up for a median of four years. IPAD tests the hypothesis that antihypertensive medications in adults with type 2 diabetes, whose seated BP 120-139 mm Hg systolic and below 90 mm Hg diastolic, results in 20% difference in the incidence of major adverse cardiovascular and cerebrovascular events. During follow-up for participants in the intensive group, the sitting systolic pressure should be decreased to below 120 mm Hg, by titration and combination of the study medications of an angiotensin type-1 receptor blocker Allisartan (240 mg/day), a dihydropyridine calcium-channel blocker (amlodipine 5-10 mg/day), and/or other medications if necessary. For those in the standard group, the sitting systolic pressure should be monitored and controlled below 140 mm Hg.

This description comes directly from the study's public registry record.

Talk to the study team

Jiyan Chen, MD  ·  86-13802911148  ·  chen-jiyan@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Guangdong General HospitalGuangzhou, Guangdong, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT03264352