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NCT03539497

Prognostic Value of Plasma Mitochondrial DNA and Cytochrome C After Cardiac Arrest

Status unknown Last updated 6 December 2023
What this trial tests

trial testing Biomarker in Cardiac Arrest in 87 participants. Status unknown.

Timeline
8 January 2019
Primary endpoint
23 August 2023
30 March 2024

Quick facts

Lead sponsorUniversity Medical Centre Ljubljana
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment87
Start date8 January 2019
Primary completion23 August 2023
Estimated completion30 March 2024
Sites1 location across Slovenia

Drugs / interventions tested

Conditions studied

Sponsor

University Medical Centre Ljubljana

Who can join

14 and older, any sex, with Cardiac Arrest. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the study is to determine prognostic value of plasma mitochondrial DNA and cytochrome C after cardiac arrest. The study will be conducted in three parts: 1. Determine plasma concentrations of mitochondrial DNA and cytochrome C in healthy population. 2. Determine release profile of mitochondrial DNA and cytochrome C to plasma after cardiac arrest. 3. Determine plasma prognostic value of mitochondrial DNA and cytochrome C after cardiac arrest and compare it with established prognostic methods.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Markers of Mitochondrial Injury and Neurological Outcomes of Comatose Patients after Cardiac Arrest.
    Živanović I, Miš K, Pirkmajer S, Marić I, et al · · 2024 · PMID 39202565 · DOI 10.3390/medicina60081286

Verify or expand the search:

Other trials of Biomarker

Trials testing the same drug.

Other recruiting trials for Cardiac Arrest

Currently open trials in the same condition.

Other University Medical Centre Ljubljana trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03539497.

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