ClinicalTrials.Veeva

Menu

Effects of Angiotensin Converting Enzyme (ACE) Inhibitors Versus Candesartan in Reducing Cardiovascular Events in Primary Treatment of Hypertension (ARBACE)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Hypertension
Cardiovascular Disease

Study type

Observational

Funder types

Industry

Identifiers

NCT01152567
NIS-CSE-ATA-2010/1

Details and patient eligibility

About

The planned Study will be a retrospective study on the effect of ACE's vs. candesartan on cardiovascular events and on health economic effects in a "real life" setting in Sweden.

Enrollment

50,000 patients

Sex

All

Ages

17+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all patients found in electronic patient journals at the participating centres, who were prescribed either ACEis (ATC-C09A-B) or ARBs (C09C-D) for hypertension from 1 January 1999 - 31 December 2007. The first date of such a prescription starts the observation time and is called the index prescription.

Exclusion criteria

  • No history of cardiovascular disease.
  • Ongoing malignancy

Trial design

50,000 participants in 2 patient groups

ACE
Description:
Patients treated for hypertension with ACEs without CVD
Candesartan
Description:
Patients treated for hypertension with candesartan without CVD

Trial contacts and locations

56

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems