Clinical Trials Directory

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UnknownNCT02214498

Treatment of HYpertension: Morning Versus Evening

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Erasmus Medical Center · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Rationale: The nocturnal blood pressure mean is an independent and stronger predictor of cardiovascular disease (CVD) risk than either daytime office, awake or 24hour mean blood pressure. In general, when nocturnal blood pressure does not decline CVD risk is higher, usually referred to as "dippers" versus "non-dippers". Evening administration of treatment might lower nocturnal blood pressure more effectively than morning administration, which is most commonly advised. The main hypothesis of this study is that evening administration of antihypertensive medication might resume the dipping pattern in non-dippers and as a consequence might reduce CVD risk more than morning administration. Primary objective (in short): -to prove that evening administration of enalapril/hydrochlorothiazide in non-dippers can resume a dipping blood pressure pattern in non-dippers Study design: A double-blind placebo-controlled cross-over study Each person will use for one period of six weeks enalapril/hydrochlorothiazide in the morning and placebo in the evening, and one period of six weeks the other way around

Conditions

Interventions

TypeNameDescription
DRUGEnalapril/hydrochlorothiazideThe intervention implies that morning and evening administration of enalapril/hydrochlorothiazide will be compared
DRUGPlacebo

Timeline

Start date
2015-05-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2014-08-12
Last updated
2014-08-15

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT02214498. Inclusion in this directory is not an endorsement.