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Short Treatment with the Angiotensin Receptor Blocker Candesartan Surveyed by Telemedicine

Not Applicable
Completed
Conditions
Hypertension
Registration Number
JPRN-UMIN000000941
Lead Sponsor
Department of Internal Medicine, School of Medicine, Keio University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
220
Inclusion Criteria

Not provided

Exclusion Criteria

Patients satisfying any one of the following criteria will be excluded from the study: 1.Secondary hypertension 2.Diabetes mellitus (HbA1c values of 6.5% or greater) 3.Renal dysfunction (serum creatinine values of 2 mg/dl or greater) 4.Patients with a history of cardiovascular disease (stroke, transient ischemic attack, coronary heart disease, heart failure) 5.Patients with severe liver dysfunction 6.Patients with malignancies 7.Pregnant patients, or patients intending to be pregnant 8.Other patients judged to be inappropriate by the attending physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Antihypertensive drug withdrawal success rates
Secondary Outcome Measures
NameTimeMethod
1. Median duration of drug withdrawal 2. Changes in home and office BP values after drug withdrawal
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