Clinical Trials Directory

Trials / Completed

CompletedNCT00534651

Paracetamol and Endothelial Function in Patients With Stable Coronary Artery Disease

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
37 (actual)
Sponsor
University of Zurich · Academic / Other
Sex
All
Age
30 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the effect of orally given paracetamol on the vascular function and on 24-hour blood pressure in patients with coronary artery disease

Detailed description

Patients with chronic pain diseases (e.g. osteoarthritis) are dependent on effective medication. NSAIDs are very effective in lowering pain in these patients. Recently there has aroused major concern with regard to cardiovascular side effects and safety, especially in selective cyclooxygenase-2 inhibitors (coxibs) but also in "regular" NSAIDs. At the moment, there is a big confusion, whether these drugs still should be used, especially in patients with known coronary artery disease. Physicians now try to switch to high dose paracetamol, despite the weaker efficacy in pain relieve, because this drug is considered generally as not harmful. As there is very few information on the cardiovascular effect of this drug, we plan to perform this study and investigate the impact of paracetamol on endothelial function, an important cardiovascular surrogate marker, on inflammatory markers and on oxidative stress in patients with coronary artery disease on top of standard medication, including aspirin

Conditions

Interventions

TypeNameDescription
DRUGParacetamolParacetamol 3x1000mg daily or Placebo for two weeks in a crossover design with a two-week washout-phase in between.

Timeline

Start date
2006-11-01
Primary completion
2010-01-01
Completion
2010-01-01
First posted
2007-09-26
Last updated
2019-12-03

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00534651. Inclusion in this directory is not an endorsement.