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Effect of Nocturnal Administration of Anti-hypertensive Medications in NoN-dippers

NCT01091753 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2010-10-08

No results posted yet for this study

Summary

The purpose of this study is to determine the effect of nocturnal administration of Anti-hypertensive medications in Non-dippers.

Efficacy variables.

1. ECHO
2. 24hr. horter
3. IMT
4. BUN/crea, urine analysis (microalbulinuria
5. Cardio vascular event. "

Conditions

Interventions

DRUG

Valsaltan, amlodipine

nti hypertensive medication time (nocturnal administration vs morning administration

Sponsors & Collaborators

  • Yonsei University

    lead OTHER

Principal Investigators

  • Dong hun Choi · professor of division of Cardiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2009-05-31
Completion
2009-09-30

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01091753 on ClinicalTrials.gov