Clinical Trials Directory

Trials / Completed

CompletedNCT01180413

Intensive Vasodilator Therapy in Patients With Essential Hypertension

Effects of Intensive Vasodilating add-on Therapy on Peripheral Vascular Resistance and Coronary Flow Reserve in Patients With Essential Hypertension

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Aarhus University Hospital · Academic / Other
Sex
All
Age
25 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether add-on of intensive vasodilator therapy can improve the coronary perfusion and reduce the total peripheral resistance in patients with ongoing treatment for essential hypertension.

Detailed description

Morphological changes are observed in the microvasculature of patients with essential hypertension. The lumen diameter is reduced in resistance arteries, but with no change in vessel cross-sectional area or wall mass. These structural changes are termed inward eutrophic remodelling and results in an increased wall:lumen ratio, caused by rearrangement of cell matrix and not by hypertrophy of smooth muscle cells in the vascular wall as observed in secondary forms of hypertension. The morphological changes also occur in the coronary arteries and cause a reduction in the ability to increase coronary perfusion as response to increased cardiac work. This is observed as a reduced coronary flow reserve in patients with sustained hypertension. Two recently published clinical studies associates an increase in media:lumen ratio with an increased risk of cardiovascular events, and it therefore seems beneficial to normalize the vascular structure in patients with essential hypertension. It has previously been demonstrated that reversion of vascular remodelling and thereby normalization of the vascular structure, requires vasodilatation and not just blood pressure reduction, suggesting that patients with essential hypertension can benefit from antihypertensive treatment aimed to induce vasodilatation. The purpose of this study is to determine whether add-on of intensive vasodilator therapy can improve the coronary perfusion (coronary flow reserve) and reduce the total peripheral resistance in patients with ongoing treatment for essential hypertension. We also aim to investigate whether changes in coronary flow reserve correlates better to changes in total peripheral resistance than changes in blood pressure. Particularly we aim to study if patients with high total peripheral resistance, despite blood pressure control, can benefit from intensive vasodilating therapy.

Conditions

Interventions

TypeNameDescription
DRUGAmlodipine5 mg per day for 6 months as add-on to original ongoing antihypertensive treatment
DRUGRamipril5 mg per day for the first to weeks as add-on to original ongoing antihypertensive treatment. Then upward adjustment to 10 mg per day for 6 months if no intolerable side effects are experienced.
DRUGLercanidipineUp to 20 mg per day for 6 months as add-on to original ongoing antihypertensive treatment
DRUGLosartanUp to 100 mg per day for 6 months as add-on to original ongoing antihypertensive treatment

Timeline

Start date
2010-12-01
Primary completion
2012-04-01
Completion
2012-04-01
First posted
2010-08-12
Last updated
2012-04-19

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01180413. Inclusion in this directory is not an endorsement.