Clinical Trials Directory

Trials / Completed

CompletedNCT01576536

Genetic Variation in Platelet Aggregation

Status
Completed
Phase
Study type
Observational
Enrollment
117 (actual)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The aim of the study is to test whether genetic variation in the alpha 2A adrenergic receptor affects diurnal variation in platelet aggregation.

Detailed description

There is a marked diurnal fluctuation in the occurrence of acute myocardial infarction and sudden death, with peak incidences occurring in the early morning. Platelet aggregation has also been shown to increase in the early morning. The investigators will test the hypothesis that alpha 2a-adrenergic receptor (ADRA2A) genetic variation, specifically haplotype 4, affects platelet aggregation. The investigators will compare diurnal platelet aggregation in haplotype 4 subjects with subjects in the other haplotype families. In addition, the investigators will compare platelet aggregation after the cold pressor test in haplotype 4 with the other haplotype families. If there are no differences among haplotypes, then the haplotypes will be combined to analyze.

Conditions

Timeline

Start date
2012-07-01
Primary completion
2015-12-01
Completion
2016-12-01
First posted
2012-04-12
Last updated
2019-06-05
Results posted
2019-06-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01576536. Inclusion in this directory is not an endorsement.

Genetic Variation in Platelet Aggregation (NCT01576536) · Clinical Trials Directory