NL-OMON20381CompletedNot Applicable
HOw feaR affects platelet aggRegability in healthy vOlunteeRs – a randomized crossover trial
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- one
- Enrollment
- 22
Study Overview
Brief Summary
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Age between 18-30 years
- •-No prior medical history (Use of contraceptive medication with monophasic oral contraceptives or an intra-uterine device (i.e. Mirena) is permitted)
Exclusion Criteria
- •-Alcohol intake within 24 hours prior to blood sampling
- •-Abnormal platelet count (i.e. <100 or > 400 x 109)
- •-NSAID intake within 24 hours prior to blood sampling
- •-Recent use of (other) antiplatelet drugs, anticoagulants or other drugs known to alter platelet function (e.g. serotonin reuptake inhibitors)
- •-Pregnancy
- •*Platelet count will be determined after the analyses of the first blood samples. If a subject turns out to have an abnormal platelet count, he or she will be excluded from the experiment.
Investigators
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