Clinical Trials Directory

Trials / Completed

CompletedNCT02148939

Antiplatelet Effects in Stroke-Patients

Dipyrone Nullifies Aspirin Antiplatelet Effects in Stroke-Patients

Status
Completed
Phase
Study type
Observational
Enrollment
61 (actual)
Sponsor
Heinrich-Heine University, Duesseldorf · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Many patients suffer from acute and chronic pain. The incidence of chronic pain correlates with increased age. Most of patients rely on analgesic medication to control the pain. Dipyrone is an extensively used drug in Western and Eastern Europe as well as Central and South America, largely due to its favorable analgesic and antipyretic effects in conjunction with a low incidence of gastrointestinal complications when compared to other non-steroidal anti-inflammatory drugs (NSAIDs). Aspirin is the backbone of antiplatelet therapy in patients after ischemic stroke. However, it is known that there are substantial inter-individual response variabilities to antiplatelet medication. Furthermore, patients with impaired response to aspirin have a significant higher risk of recurrent cerebrovascular events. The investigators have recently shown that co-medication with aspirin and dipyrone in patients with coronary artery disease lead to insufficient antiplatelet effects of aspirin. The incidence of chronic pain is very high in patients with ischemic stroke. Therefore, in this study the investigators aim to examine, if co-medication of aspirin and dipyrone interaction also occurs in patients after ischemic stroke.

Conditions

Timeline

Start date
2014-05-01
Primary completion
2015-02-01
Completion
2015-02-01
First posted
2014-05-29
Last updated
2015-03-10

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02148939. Inclusion in this directory is not an endorsement.