Clinical Trials Directory

Trials / Completed

CompletedNCT03276598

A Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension

A Randomised Double-blind Cross-over Single-centre Study on Molecular Genetics of Drug Responsiveness in Essential Hypertension

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
233 (actual)
Sponsor
Helsinki University Central Hospital · Academic / Other
Sex
Male
Age
35 Years – 59 Years
Healthy volunteers
Not accepted

Summary

Blood pressure variation and the risk of essential hypertension have an important genetic component. In most cases susceptibility to essential hypertension is likely determined by the action of more than one gene. The identification of genes causing susceptibility to hypertension is important, since it would give new tools for the diagnosis and enable better etiological classification and specific treatment of the disease. The innovation of this study is to use the response to antihypertensive therapy as an intermediate phenotype. In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor antagonist and a calcium channel blocker. The drugs that are selected for the study are "typical" representatives of their groups and long-acting, and the dosages are sufficient but well tolerable.

Detailed description

Blood pressure variation and the risk of essential hypertension have an important genetic component. In most cases susceptibility to essential hypertension is likely determined by the action of more than one gene. The identification of genes causing susceptibility to hypertension is important, since it would give new tools for the diagnosis and enable better etiological classification and specific treatment of the disease. Finland is an ideal place for a study like this because of the genetic homogeneity of the population, the relatively high prevalence of the disease and the established protocols for the treatment and follow-up of hypertension in public health care. The molecular genetic studies on hypertension performed so far (by 1999) have primarily been association studies, which are based on case-control classification and may produce erroneous results. Particularly, a reliable phenotyping of cases and controls has been difficult. Consequently, more attention should be paid to the phenotyping of patients, and novel intermediate phenotypes characteristic of certain subtypes of hypertension should be used to facilitate the search for hypertension genes. The innovation of this study is to use the response to antihypertensive therapy as an intermediate phenotype. In the study, each subject uses one of four antihypertensive drugs, each as a monotherapy in a rotational fashion, for 28 days in a randomized order. The antihypertensive drugs to be tested include a thiazide diuretic, a beta-adrenergic antagonist, an angiotensin-II receptor antagonist and a calcium channel blocker. The drugs that are selected for the study are "typical" representatives of their groups and long-acting, and the dosages are sufficient but well tolerable. The study design does not necessitate the use of equipotent doses of the various agents, since the study is not designed to compare the antihypertensive effectiveness of the study drugs or, due to the short treatment periods, their effects on clinical endpoints.

Conditions

Interventions

TypeNameDescription
DRUGAmlodipineTreatment for four weeks. Dose: 5 mg o.d.
DRUGBisoprololTreatment for four weeks. Dose: 5 mg o.d.
DRUGHydrochlorothiazideTreatment for four weeks. Dose: 25 mg o.d.
DRUGLosartanTreatment for four weeks. Dose: 50 mg o.d.
DRUGPlaceboTreatment for four weeks. Dose: 1 tablet per day.

Timeline

Start date
1999-11-25
Primary completion
2004-04-01
Completion
2004-04-01
First posted
2017-09-08
Last updated
2017-09-11

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT03276598. Inclusion in this directory is not an endorsement.