Status:

TERMINATED

Effects of Intensive Long-Term Vasodilation in Hypertensive Patients With Microvascular Angina Pectoris

Lead Sponsor:

University of Aarhus

Collaborating Sponsors:

Danish Cardiovascular Research Academy

Danish Heart Foundation

Conditions:

Microvascular Angina

Hypertension

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to determine if long-term vasodilatory treatment is more effective than the standard treatment in hypertensive patients with microvascular angina pectoris

Detailed Description

Patients with hypertension frequently develop angina pectoris. This can be caused by either epicardial stenotic disease or, equally frequent, by increased resistance in small resistance vessels - micr...

Eligibility Criteria

Inclusion

  • hypertension
  • angina pectoris CCS class II-IV
  • objective signs of ischemia on exercise-ECG or myocardial SPECT
  • no significant stenosis on angiography (minimal lumen diameter \>50% of relevant reference segment)

Exclusion

  • known allergy to any study medication
  • abnormal lab tests of clinical significance
  • valvular disease of haemodynamic significance
  • known secondary hypertension
  • atrial fibrillation or other significant arrythmias
  • myocardial infarction \< 30 days before inclusion
  • resting angina \< one week before inclusion
  • known endocrine disease, nephropathy or hepatic disease
  • present malignant disease
  • pregnancy
  • fertile women not using safe contraceptives \> 6 months before inclusion. Use of contraceptives must continue 1 month after completion or retraction from the study
  • body mass index \> 30
  • significant chronic obstructive lung disease (FEV1 \< 1.5 l)
  • participant in another study including test medicine
  • present treatment with dipyridamole
  • present treatment with phosphodiesterase-5-inhibitors that the patient does not want to discontinue during the study period
  • heart transplanted patients
  • patients with magnetizable metallic implants

Key Trial Info

Start Date :

January 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2008

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT00424801

Start Date

January 1 2007

End Date

December 1 2008

Last Update

May 6 2009

Active Locations (1)

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1

Aarhus Hospital

Aarhus, Denmark, 8000