HEALTHY VOLUNTEERS K50.9 K51.9 A04.8
Conditions
Interventions
Group 1: Patients with Crohn's disease
Phase 1: Case-Control
Measurement of PoP concentrations in plasma, platelets and stools at point of diagnosis.
Phase 2: Longitudinale Phase
Measurement of P
Sponsors
Medizinische Universität Graz
Eligibility
Sex/Gender
All
Age
No minimum to 18 Years
Inclusion criteria
Inclusion criteria: Written informed consent, pediatric patients suspicious for CED or bacterial intestinal infection or volunteers (healthy and normal clotting and aggregation tests)
Exclusion criteria
Exclusion criteria: missing written consent, anticoagulant therapy (e.g. Heparin) or antiplatelet therapy (e.g. Aspirin or Clopidogrel)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome is the concentration of inorganic polyphosphates in plasma. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome is the levels of polyphosphates in platelets and stools. | — |
Countries
Austria
Contacts
Public ContactHarald Haidl
Universitätsklinik für Kinder- und JugendheilkundeMedizinische Universität Graz
Outcome results
None listed