Systemic and local inflammation in burn wound patients.
Completed
- Conditions
- partial and full-thickness burns10014982
- Registration Number
- NL-OMON47865
- Lead Sponsor
- Rode Kruis Ziekenhuis
- Brief Summary
Trial ended prematurely
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 83
Inclusion Criteria
Patient group
>=18 years
Competent and temporarily incompetent patients
Informed Consent by patient or the legal representative
No acute psychiatric disorders
Speak sufficient Dutch'
Healthy volunteers:
18 years or older
competent
informent consent
sufficient dutch proficiency
Exclusion Criteria
patients:
See inclusion criteria
Healty volunteers:
any medication exept contraceptives
known underlying diseases as cancer, inmune deficiency, hypertension, complement disorder
Study & Design
- Study Type
- Observational invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method