Clinical Trials Directory

Trials / Completed

CompletedNCT00159718

Double Blind Atorvastatin Amlodipine Study

Double Blind Atorvastatin Amlodipine Study (DUAAL) Effect Of Amlodipine, Atorvastatin And The Combination On Transient Myocardia Ischemia In Coronary Artery Disease.

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
360 (planned)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
All
Age
21 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To evaluate and compare the safety and efficacy of amlodipine, atorvastatin and the combination in patients with symptomatic myocardial ischemia. Amlodipine's use in angina has been well documented in clinical trials such as the Circadian Anti-Ischemia Program in Europe (CAPE), but the impact on vascular inflammation in clinical practice has not been tested. Furthermore, the potentially synergistic benefit of atorvastatin and amlodipine on inflammation ischemic activity has not been studied.

Conditions

Interventions

TypeNameDescription
DRUGamlodipine
DRUGatorvastatin

Timeline

Start date
2001-07-01
Completion
2007-01-01
First posted
2005-09-12
Last updated
2021-01-28

Locations

33 sites across 11 countries: Croatia, Czechia, Estonia, Hungary, Latvia, Norway, Poland, Romania, Slovakia, South Africa, Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT00159718. Inclusion in this directory is not an endorsement.

Double Blind Atorvastatin Amlodipine Study (NCT00159718) · Clinical Trials Directory