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Metabolomic Profiling of Patients With Traumatic Brain Injury

Metabolomic Profiling of Patients With Traumatic Brain Injury

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07292766
Enrollment
60
Registered
2025-12-18
Start date
2024-02-01
Completion date
2026-02-01
Last updated
2025-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury, Traumatic Brain Injury (TBI) Patients

Keywords

traumatic brain injury, metabolomics

Brief summary

Traumatic Brain Injury (TBI) is a significant cause of mortality and morbidity worldwide. However, the literature on determining its severity and predicting prognosis is insufficient. This study aimed to examine the differences in metabolite levels between trauma patients with severe TBI and orthopedic trauma patients without brain injury.

Detailed description

Traumatic Brain Injury (TBI) is a significant cause of mortality and morbidity worldwide, particularly in young people. TBI is a complex metabolic process associated with an energy crisis resulting from multiple mechanisms, including ischemia, diffusion hypoxia, and mitochondrial dysfunction. Because metabolic derangement is a fundamental component of TBI pathophysiology, these metabolic changes may provide prognostic information and guide treatment. Additionally, the release of brain-specific metabolites (i.e., small molecules with a molecular mass below 500 Da) into the systemic circulation may provide insights into blood-brain barrier (BBB) dysfunction, a fundamental process in TBI. Metabolomic profiling studies are introductory and valuable for elucidating this metabolic process.

Interventions

None listed

Sponsors

Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Ages 18-65 * Patients diagnosed with severe TBI clinically or according to National Institute for Health and Care Excellence (NICE) criteria (including post-traumatic imaging) * Patients with non-TBI orthopedic or multitrauma

Exclusion criteria

* Presence of brain pathology in the pre-trauma period * Patient with chronic subdural hematoma

Design outcomes

Primary

MeasureTime frameDescription
metabolomic analysisDay 1Venous blood samples are taken from the participants after the injury. Samples will be analysed using LC/MS. All relevant metabolomes and their respective metabolic pathways will be evaluated using the KEGG Pathway database.

Countries

Turkey (Türkiye)

Contacts

Primary ContactHazal Ekin AYTUĞ, Consultant anesthesiologist
drekinguran@gmail.com+905078448449

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026