Intensive Vasodilator Therapy in Patients With Essential Hypertension (Vasomore)
Primary Purpose
Essential Hypertension, High Blood Pressure
Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Amlodipine
Ramipril
Lercanidipine
Losartan
Sponsored by
About this trial
This is an interventional treatment trial for Essential Hypertension focused on measuring Inward eutrophic remodelling
Eligibility Criteria
Inclusion Criteria:
- Ongoing antihypertensive treatment for >3 months
- Blood pressure >120/75 during antihypertensive treatment
- Ejection fraction > 45%
Exclusion Criteria:
- Blood pressure >160/100
- Pregnancy
- fertile women not using safe contraceptives
- known secondary hypertension
- valvular disease of haemodynamic significance
- known endocrine disease, nephropathy or hepatic disease
- present malignant disease
- known psychiatric disease
- abnormal lab tests of clinical significance
- known allergy to any study medication
- body mass index > 35
- Ongoing antihypertensive treatment with a combination of ACE-inhibitor and Calcium antagonist.
Sites / Locations
- Aarhus University Hospital - dept. cardiology (A)
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Vasodilatory
Arm Description
Patients in this arm will receive intensive vasodilatory treatment
Outcomes
Primary Outcome Measures
Coronary Flow Reserve
Determined by echocardiography
Secondary Outcome Measures
Puls Wave Velocity
Left ventricular mass
Determined with echocardiography
Blood Pressure
Ambulatory Blood Pressure
Peripheral Vascular Resistance
By Innocor
Minimal forearm vascular resistance
By pletysmography
Full Information
NCT ID
NCT01180413
First Posted
August 11, 2010
Last Updated
April 18, 2012
Sponsor
Aarhus University Hospital
Collaborators
University of Aarhus
1. Study Identification
Unique Protocol Identification Number
NCT01180413
Brief Title
Intensive Vasodilator Therapy in Patients With Essential Hypertension
Acronym
Vasomore
Official Title
Effects of Intensive Vasodilating add-on Therapy on Peripheral Vascular Resistance and Coronary Flow Reserve in Patients With Essential Hypertension
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
December 2010 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aarhus University Hospital
Collaborators
University of Aarhus
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Essential Hypertension, High Blood Pressure
Keywords
Inward eutrophic remodelling
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
48 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vasodilatory
Arm Type
Experimental
Arm Description
Patients in this arm will receive intensive vasodilatory treatment
Intervention Type
Drug
Intervention Name(s)
Amlodipine
Other Intervention Name(s)
Amlodipin
Intervention Description
5 mg per day for 6 months as add-on to original ongoing antihypertensive treatment
Intervention Type
Drug
Intervention Name(s)
Ramipril
Intervention Description
5 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.
Intervention Type
Drug
Intervention Name(s)
Lercanidipine
Intervention Description
Up to 20 mg per day for 6 months as add-on to original ongoing antihypertensive treatment
Intervention Type
Drug
Intervention Name(s)
Losartan
Intervention Description
Up to 100 mg per day for 6 months as add-on to original ongoing antihypertensive treatment
Primary Outcome Measure Information:
Title
Coronary Flow Reserve
Description
Determined by echocardiography
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Puls Wave Velocity
Time Frame
6 months
Title
Left ventricular mass
Description
Determined with echocardiography
Time Frame
6 months
Title
Blood Pressure
Description
Ambulatory Blood Pressure
Time Frame
6 months
Title
Peripheral Vascular Resistance
Description
By Innocor
Time Frame
6 months
Title
Minimal forearm vascular resistance
Description
By pletysmography
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Ongoing antihypertensive treatment for >3 months
Blood pressure >120/75 during antihypertensive treatment
Ejection fraction > 45%
Exclusion Criteria:
Blood pressure >160/100
Pregnancy
fertile women not using safe contraceptives
known secondary hypertension
valvular disease of haemodynamic significance
known endocrine disease, nephropathy or hepatic disease
present malignant disease
known psychiatric disease
abnormal lab tests of clinical significance
known allergy to any study medication
body mass index > 35
Ongoing antihypertensive treatment with a combination of ACE-inhibitor and Calcium antagonist.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Morten Engholm Pedersen, MD
Organizational Affiliation
Aarhus University and Aarhus University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ole Norling Mathiasen, MD, PhD
Organizational Affiliation
Aarhus University and Aarhus University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Niels Henrik Buus, DMSc
Organizational Affiliation
Aarhus University and Aarhus University Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ashkan Eftekhari, MD, PhD
Organizational Affiliation
Aarhus University and Aarhus University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Aarhus University Hospital - dept. cardiology (A)
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
Learn more about this trial
Intensive Vasodilator Therapy in Patients With Essential Hypertension
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