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Clinical Trials/EUCTR2016-004303-32-NL
EUCTR2016-004303-32-NL
Active, not recruiting
Phase 1

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

VU university medical center0 sites62 target enrollmentApril 13, 2017

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Hyperaggregability of thrombocytes triggered by severe infection (i.e. pneumonia or invasive urinary tract infection or a cutaneous infection).
Sponsor
VU university medical center
Enrollment
62
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 13, 2017
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
VU university medical center

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:
  • Primary clinical diagnosis of pneumonia
  • Primary clinical diagnosis of invasive urinary tract infection

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
  • \-Currently pregnant

Outcomes

Primary Outcomes

Not specified

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