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Clinical Trials/NL-OMON50157
NL-OMON50157
Completed
Phase 4

ASsesment of Platelet function and Inhibition in patients Recovering from severe INfection - ASPIRIN-trial

Vrije Universiteit Medisch Centrum0 sites97 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Acute myocardial infarction
Sponsor
Vrije Universiteit Medisch Centrum
Enrollment
97
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • In order to be eligible to participate in the main\-trial, a subject must meet
  • all of the following criteria:
  • Primary clinical diagnosis of pneumonia
  • Primary clinical diagnosis of invasive urinary tract infection
  • Primary clinical diagnosis of cutaneous infection
  • 18 years or older on the date of hospital presentation
  • Hospitalization for at least 24 hours
  • Having received at least 1 dose of antibiotics within 48 hours of admission.
  • In order to be eligible to participate in the sub\-study, a subject must meet
  • all of the following criteria:

Exclusion Criteria

  • A potential subject who meets any of the following criteria will be excluded
  • from participation in the main\-trial:
  • \- Active metastatic cancer (c.q. malignancy)
  • \- Allergy to salicylate
  • \- Platelet count \<120\*109/l
  • \- History of non\-traumatic major bleeding
  • \- Known bleeding diathesis
  • \- Conditions which require antiplatelet therapy
  • \- Usage of antiplatelet therapy
  • \- Surgery 1 month prior to diagnosis

Outcomes

Primary Outcomes

Not specified

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