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Doxazosin and Ramipril in Hypertension

Phase 4
Completed
Conditions
Hypertension
Interventions
Registration Number
NCT02901977
Lead Sponsor
Karolinska Institutet
Brief Summary

Randomized double-blind parallel group study in patients with mild-to-moderate hypertension to evaluate the effects beyond the blood pressure lowering effect of treatment for 12 weeks with ramipril or doxazosin on hemostatic mechanisms and on endothelial function.

Detailed Description

This study aims to answer the following questions: 1) Does antihypertensive therapy with doxazosin exhibit antithrombotic effects in patients with essential hypertension? 2) Are the potential antithrombotic effects of doxazosin different to the effects of an ACE inhibitor? 3) Is there a relation between the antihypertensive effect and the antithrombotic effect of these antihypertensive agents?

The co-primary outcomes are changes in endothelial function assessed by flow mediated vasodilatation, and in haemostatic function measured by the generation of thrombin-antithrombin complex.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
71
Inclusion Criteria
  • Primary mild-to-moderate hypertension
Exclusion Criteria
  • Pregnancy and lactation
  • Recent (6 months) malignant disease or ongoing treatment for malignancy
  • No absolute indication or contraindication for any of the study drugs

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Alpha receptor blockerDoxazosinDoxazosin tablets 8 mg od for 12 weeks
ACE inhibitorRamiprilRamipril tablets 10 mg od for 12 weeks
Primary Outcome Measures
NameTimeMethod
Thrombin generation12 weeks

Thrombin-Antithrombin complex (TAT)

Endothelial function12 weeks

Forearm post-ischemic flow mediated dilatation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Karolinska Institutet, Daprtment of Clinical Sciences, Danderyd Hospital, Cardiovascular Research Laboratory

🇸🇪

Stockholm, Sweden

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