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

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age45-79
SponsorXueQing Yu

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

irrespective of sex;

aged between 45 and 79 years;

with office-measured seated BP 120-139 mm Hg systolic and below 90 mm Hg diastolic;

diagnosed of type 2 diabetes mellitus (T2DM), currently on diabetic therapy;

Disqualifiers

poor control of blood glucose, HbA1c > 10.0%

administration of any antihypertensive medications within 1 month;

a history of hypoglycemic coma / seizure;

confirmed diagnosis of type 1 diabetes mellitus;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Allisartan Isoproxil

    Drug

    Allisartan Isoproxil 240mg daily will be used to lower BP to below 120 mm Hg systolic.

  • Amlodipine 5mg

    Drug

    Amlodipine 5mg daily will be added to Allisartan Isoproxil and afterwards increased to 10mg daily, if necessary to reach the blood pressure goal (below 120 mm Hg systolic).

  • Standard treatment by current guideline

    Other intervention

    No BP-lowering medications are used until BP becomes ≥ 140 mm Hg systolic and/or 90 mm Hg diastolic. Medications are determined by investigators in lines with recommendations by current Chinese guidelines to decrease BP to lower than 140 mm Hg systolic and to lower than 90 mm Hg diastolic.

Treatment groups

11,414 Participants
are divided into 2 treatment groups
Group A: intensive treatment groupActive comparator 2 interventions
Group B: standard treatment groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Composite of Major Adverse Cardiovascular and Cerebrovascular Events

The major adverse cardiovascular and cerebrovascular events defined in the study include cardiovascular death, nonfatal stroke, nonfatal myocardial infarction, hospitalization for congestive heart failure and hospitalization for unstable angina.

Time frame
From date of randomization until the date of first documented incidence of the major adverse cardiovascular events prespecified, whichever comes first, assessed up to 60 months

Secondary outcomes

1

Stroke

Stroke (ICD-Code I60, I61, I63, I64) is a focal neurological deficit with symptoms continuing for more than 24 hours or leading to death with no apparent cause other than vascular. Stroke as an endpoint in IPAD includes definite ischemic stroke, primary intracerebral hemorrhage and subarachnoid hemorrhage with evidence from CT or MRI scan within 14 days of onset or autopsy confirmation, and stroke of unknown type etiology when CT, MRI, or autopsy are not done and information is inadequate to diagnose the etiology definitely.

Time frame
From date of randomization until the date of first documented incidence of stroke, assessed up to 60 months.
2

Cardiovascular Death

Cardiovascular death include death caused by stroke, MI, HF, sudden death or any other death attributed to cardiovascular diseases. Sudden death (ICD-Code I46.1, R96) encompasses any death of unknown origin occurring instantly or within an estimated 24 hours after the onset of acute symptoms as well as unattended death for which no likely cause can be established by autopsy or recent medical history.

Time frame
From date of randomization until the date of cardiovascular death, assessed up to 60 months.
3

Acute Myocardial Infarction

Acute myocardial infarction (MI) (ICD-Code I21) is defined when any one of the following criteria occurs. (1) Detection of a rise and/or fall of cardiac biomarker values, with at least one value above the 99th percentile upper reference limit and with at least one of the following manifestations: symptoms of ischaemia that should have lasted for at least 30 minutes and should not have been responsive to sublingual administration of nitrates; new or presumed new significant ST-segment-T wave changes or new left bundle branch block (LBBB); development of pathological Q waves in the ECG; imaging evidence of new loss of viable myocardium or new regional wall motion abnormality. (2) Identification of an intracoronary thrombus by angiography or autopsy. (3) Cardiac death with symptoms suggestive of myocardial ischaemia and presumed new ischaemic ECG changes or new LBBB, but death occurred before cardiac biomarkers were obtained, or before cardiac biomarker values would be increased.

Time frame
From date of randomization until the date of first documented incidence of acute MI, assessed up to 60 months.
4

Hospitalization of Unstable Angina

Unstable angina (ICD-Code I20.0) is defined as new onset or worsening angina pectoris requiring hospitalization with angiographically documented coronary atherosclerosis or transient electrocardiographic changes of the ST-segment or T-wave without evidence for myocardial necrosis. This diagnosis excludes patients with angina pectoris admitted to the hospital only for investigation.

Time frame
From date of randomization until the date of first documented hospitalization of unstable angina, assessed up to 60 months.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

XueQing Yu

Lead sponsor

Guangdong Provincial People's Hospital

Sponsor institution