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Doxazosin and Ramipril in Hypertension

On the Antithrombotic Effects of Doxazosin and Ramipril in Essential Hypertension

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02901977
Acronym
DoRa
Enrollment
71
Registered
2016-09-15
Start date
2011-03-31
Completion date
2015-04-30
Last updated
2025-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Hypertension, Blood pressure, Hemostasis, Endothelial function

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.

Interventions

DRUGRamipril

Antihypertensive therapy

DRUGDoxazosin

Antihypertensive therapy

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Thrombin generation12 weeksThrombin-Antithrombin complex (TAT)
Endothelial function12 weeksForearm post-ischemic flow mediated dilatation

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026