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Mitochondrial Dysfunction in Trauma-related Coagulopathy

P

Petra Hartmann MD Ph.D.

Status

Unknown

Conditions

Trauma Induced Coagulopathy

Treatments

Diagnostic Test: Viscoelastic assays and aggregometry tests

Study type

Observational

Funder types

Other

Identifiers

NCT05004844
5500/2021-SZTE

Details and patient eligibility

About

Bleeding control often poses a great challenge for clinicians due to trauma-induced blood clotting disorder (TIC), a condition that is present in one-third of bleeding trauma patients. As platelets are considered as central mediators in TIC, the understanding of mitochondria-mediated processes in thrombocytes may disclose new therapeutic targets in the management of severely injured patients. The investigators hypothesize that mitochondrial dysfunction occurs in the platelets of trauma patients with TIC. The investigators intend to quantitatively characterize the derangements of mitochondrial functions in TIC; and assess the relation between mitochondrial respiration and clinical markers of platelet function

Full description

Hemorrhage control often poses a great challenge for clinicians due to trauma-induced coagulopathy (TIC), a condition that is present in one-third of bleeding trauma patients. As platelets are considered as central mediators in TIC, the understanding of mitochondria-mediated processes in thrombocytes may disclose new therapeutic targets in the management of severely injured patients. The investigators hypothesize that mitochondrial dysfunction occurs in the platelets of trauma patients with TIC. The investigators intend to quantitatively characterize the derangements of mitochondrial functions in TIC; and assess the relation between mitochondrial respiration and clinical markers of platelet function measured with aggregometry, viscoelastic tests and conventional laboratory analysis.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Trauma patients
  • Injury Severity Score (ISS) 16 or greater,
  • age of 18 years or greater,
  • hemorrhage confirmed with extended focused assessment with sonography in trauma (eFAST) or computer tomography (CT)

Exclusion criteria

Trial contacts and locations

1

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Central trial contact

Péter Dr. Jávor, M.D.; Petra Dr. Hartmann, MD, Ph.D.

Data sourced from clinicaltrials.gov

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