NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000001890

Registered date:20/04/2009

Clinical trial to investigate the effect of candesartan on QOL and geriatric syndome in elderly hypertensive patients

Basic Information

Recruitment status Complete: follow-up complete
Health condition(s) or Problem(s) studiedessential hypertension
Date of first enrollment2009/04/01
Target sample size1000
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)Candesartan will be replaced with calcium channel blockers (Group A), or will be added to calcium channel blockers (Group B), depending on the blood pressure control as decided by attending physician. Candesartan can be increased up to 12 mg/day according to blood pressure.

Outcome(s)

Primary OutcomeChanges of QOL questionnaire score (SF-8)
Secondary Outcome1) Subjective symptoms of the geriatric syndrome questionnaire. 2) Office blood pressure and pulse rate. 3) Home blood pressure and pulse rate

Key inclusion & exclusion criteria

Age minimum65years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1) Subjects with irritation to candesartan 2) Subjects with (possible) pregnancy 3) Subejects with renal artery stenosis 4) Subjects with hyperkalemia 5) Subjects taking any angiotensin receptor blockers 6) Subjects who are unable to fill out the questionnaire 7) Other ineligible subjects

Related Information

Contact

public contact
Name Masahiro Akishita
Address Japan
Telephone
E-mail
Affiliation University of Tokyo Hospital Department of Geriatric Medicine
scientific contact
Name Yasuyoshi Ouchi
Address 7-3-1 Hongo, Bunkyo-ku Tokyo Japan
Telephone 03-3815-5411
E-mail
Affiliation University of Tokyo Hospital Department of Geriatric Medicine