Effect of Nocturnal Administration of Anti-hypertensive Medications in NoN-dippers
NCT ID: NCT01091753
Last Updated: 2010-10-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
28 participants
INTERVENTIONAL
2008-03-31
2009-09-30
Brief Summary
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Efficacy variables.
1. ECHO
2. 24hr. horter
3. IMT
4. BUN/crea, urine analysis (microalbulinuria
5. Cardio vascular event. "
Detailed Description
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Conditions
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Study Design
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RANDOMIZED
TREATMENT
NONE
Study Groups
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morning administration group
Valsaltan, amlodipine
nti hypertensive medication time (nocturnal administration vs morning administration
nocturnal administration group
Valsaltan, amlodipine
nti hypertensive medication time (nocturnal administration vs morning administration
Interventions
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Valsaltan, amlodipine
nti hypertensive medication time (nocturnal administration vs morning administration
Eligibility Criteria
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Inclusion Criteria
2. 24hr. holer : non-dipper
3. Age 18 \~70.
Exclusion Criteria
2. Renal failure , creatinine \>2.0mg/dl
3. Liver disease
18 Years
70 Years
ALL
No
Sponsors
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Yonsei University
OTHER
Responsible Party
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Yonsei University, College of Medicine
Principal Investigators
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Dong hun Choi
Role: PRINCIPAL_INVESTIGATOR
professor of division of Cardiology
Locations
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Severance Hospital, Yonsei University College of Medicine
Seoul, , South Korea
Countries
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Other Identifiers
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4-2007-0440
Identifier Type: -
Identifier Source: org_study_id