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Recruiting NCT05609123

Endothelial Glycocalyx Damage in Brain Death Organ Donors

Observational Brain Damage Due to Hypoxia Organ Donors Organ Transplant Failure or Rejection

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Endothelial glycocalyx damage assessment.
Who it may be relevant to
Registry conditions: Brain Damage Due to Hypoxia, Organ Donors, Organ Transplant Failure or Rejection. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Czechia
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Endothelial Glycocalyx Status and Damage in Brain Death Organ Donors

Overview

The study aims the assessment of endothelial glycocalyx (EG) degradation in deceased organ donors. There is a lack of organs for the transplantation program. By the description of the EG status, we can open room for organ optimization before transplantation and improve the organ function after transplantation in marginal donors.

Interventions

  • Diagnostic test Endothelial glycocalyx damage assessment
    Degradation products of endothelial glycocalyx will be assessed in the blood and urine.

Primary outcome measures

  • Markers of endothelial glycocalyx damage [Time frame: baseline at the time of inclusion]

Eligibility criteria

Inclusion criteria

  • patients in critical condition declared as brain dead by clinical examination

Exclusion criteria

  • N/A

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Czechia · 1 center
  • University Hospital Hradec Kralove — Hradec Králové

Identifiers

NCT: NCT05609123 · CooperatioUK_DBD_GCX

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗