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Toyama antihypertensive therapy with Olmesartan in Post-Stroke patients (TOPS) study

Phase 4
Recruiting
Conditions
Hypertension, Post-stroke
Registration Number
JPRN-UMIN000009790
Lead Sponsor
niversity of Toyama
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

Myocardial infarction, cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage, unknown type of stroke within previous 6 months (TIA can be registerd) Grade III hypertension (systolic BP>=180mmHg or diastolic BP>=110mmHg) Percutaneous or surgical coronary intervention (PCI, CABG etc.), severe heart failure within 6 months Percutaneous or surgical coronary intervention planned Persistent or permanent atrial fibrillation History of congenital heart disease, rheumatic heart disease, moderate or severe valvular heart disease Unstable angina, severe arrhythmia Pregnant, possible to pregnancy Not appropriate to long term observation Difficult to obtain consent because of minors or dementia etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Evaluation at 12 week and 24 week after 1) Blood pressure self-measured at home (home BP) in the early morning and evening, Morning/Evening ratio 2) Blood pressure at hospital (hospital BP) 3) The achievement rate of target blood pressures (at hospital and home)
Secondary Outcome Measures
NameTimeMethod
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