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Treatment of HYpertension: Morning Versus Evening

Phase 4
Conditions
Essential Hypertension
Interventions
Drug: Enalapril/hydrochlorothiazide
Drug: Placebo
Registration Number
NCT02214498
Lead Sponsor
Erasmus Medical Center
Brief 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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
120
Inclusion Criteria
  • Essential hypertension
  • Stable blood pressure on treatment with Angiotensin Converting Enzyme Inhibitor (ACEI) or Angiotensin II Receptor Blocker (ARB) and hydrochlorothiazide
  • Age between 18 and 85 years
  • WHO performance status 0-1
  • Available for a time period of 15 weeks
  • Written informed consent
  • Dippers: Nocturnal blood pressure fall of 10-20% of daytime values.20
  • Non-dippers: -Nocturnal blood pressure fall of <10% of daytime values
Exclusion Criteria
  • secondary cause of hypertension
  • use of ARB because of intolerability (e.g. dry cough) of ACEI
  • nocturnal blood pressure fall of >20% or rise
  • renal insufficiency (GFR<60 ml/min)
  • shift work
  • pregnancy or wish to get pregnant
  • use of other antihypertensive medication than ACEI, ARB, hydrochlorothiazide or a calcium channel blocker
  • use of sleeping medication

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Enalapril/hydrochlorothiazideEnalapril/hydrochlorothiazideThis arm will start with six weeks of administration of enalapril/hydrochlorothiazide in the evening and placebo in the morning, followed by six weeks of active treatment in the morning and placebo in the evening
PlaceboEnalapril/hydrochlorothiazideThis arm will start with six weeks of morning administration of enalapril/hydrochlorothiazide in the morning and placebo in the evening, followed by six weeks of placebo in the morning and active treatment in the evening
Enalapril/hydrochlorothiazidePlaceboThis arm will start with six weeks of administration of enalapril/hydrochlorothiazide in the evening and placebo in the morning, followed by six weeks of active treatment in the morning and placebo in the evening
PlaceboPlaceboThis arm will start with six weeks of morning administration of enalapril/hydrochlorothiazide in the morning and placebo in the evening, followed by six weeks of placebo in the morning and active treatment in the evening
Primary Outcome Measures
NameTimeMethod
Average nocturnal blood pressure, percentage dipping and nadir of nocturnal blood pressure24 hours

At the end of each treatment period of six weeks, a 24 hour ambulatory blood pressure measurement will be performed

Secondary Outcome Measures
NameTimeMethod
Percentage of nocturnal diastolic blood pressure measurements below 65 mm hg24 hours

One safety issue on evening administration of antihypertensive treatment is that blood pressure might get too low. We will assess this especially in the dippers.

Urine: Sodium, potassium, protein, melatonin, creatininTwo times within 24 hours at the end of six weeks of treatment according to one of the two regimes

Excretion of sodium, potassium, protein and melatonin depend on the circadian clock. Therefore, differences between morning and evening administration of antihypertensive medication are tested

Plasma: enalapril, cortisol, melatonin, aldosterone, ACE activity, gene expression of clock genesMoring of 24 hour blood pressure measurement after six weeks of treatment according to a certain regime

Trial Locations

Locations (1)

Erasmus MC

🇳🇱

Rotterdam, Netherlands

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