partial and full-thickness burns
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
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
Exclusion criteria: patients: See inclusion criteria Healty volunteers: any medication exept contraceptives known underlying diseases as cancer, inmune deficiency, hypertension, complement disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main objectives are to analyse components of the complement system and inflammatory cells involved in the different inflammatory mechanisms and systems described above. These include complement C3, C4, C5 and NETs levels (cell free DNA (cfDNANA)) in blood at different time points between day 0 and 30 pb and when the patient has to undergo escharectomy in eschar obtained at the day of surgical procedure. Timeframes for analyses are: day 0, 3-6, 7-14 and 21- 30. The latter time points will only apply for patients with more severe burn wounds and hospitalisation during the entire period. The analysis will be performed by ELISA. In addition complement (e.g. C3, C4, C5) as well as neutrophils (MPO), macrophages (CD68), lymphocytes (CD45), thrombi (CD31), NETosis (H3 histon citrulline), tissue factor (TF) and dipeptidyl peptidase 4 (DPP4/CD26) will be analysed in burned tissue samples (eschar collected at the day of the planned surgical procedure) by using (immuno) histochemistry for the cells and FACS analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| - | — |
Countries
Netherlands