Skip to content

Correcting Platelet Dysfunction After Traumatic Brain Injury

Correction of Platelet Dysfunction Following Traumatic Brain Injury in Geriatric Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03182946
Enrollment
147
Registered
2017-06-09
Start date
2017-10-01
Completion date
2021-07-01
Last updated
2022-04-21

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

Conditions

Platelet Dysfunction, Traumatic Brain Injury

Brief summary

This study evaluates the impact of platelet transfusion on geriatric patients with platelet dysfunction from Traumatic Brain Injury. The authors hypothesize that patients will recover better if their platelet dysfunction is corrected with platelet transfusion.

Detailed description

The geriatric population is subject to traumatic brain injury, often occurring as a result of falls. This patient population is also often receiving anticoagulants and platelet inhibitors increasing their risk of post-injury hemorrhage. Following Traumatic Brain Injury, even without platelet inhibitor medications, platelets become dysfunctional and are no longer able to assist with clot formation. Therefore risk of hemorrhage is increased, both in the brain, and other hemorrhagic sites. Clinical practice at Carolinas Medical Center is to transfuse platelets in patients with platelet dysfunction following brain injury. The current study is investigating the impact of transfusion on correction of platelet dysfunction and patient outcome. Furthermore, stored platelet dysfunction can be corrected by supplementation with cytochrome c, which supports mitochondrial function. Therefore, the ability of cytochrome c to correct dysfunction in ex vivo platelets from patients with Traumatic Brain Injury will be assessed.

Interventions

DIAGNOSTIC_TESTPlatelet mapping Thromboelastography

These diagnostic tests will be acquired in patients with brain injury, to determine prediction of clinical, functional and psychological outcome.

Sponsors

Carolinas Medical Center
CollaboratorOTHER
Wake Forest University Health Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Traumatic brain injury with Glasgow Coma Scale Score (GCS) \<=13

Exclusion criteria

Previously know coagulation dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Change in platelet functionWithin 5 hoursCorrection of platelet inhibition measured before and after transfusion through platelet mapping thromboelastography

Secondary

MeasureTime frameDescription
Mortality1-3 monthsMortality will be compared to admission platelet inhibition
Functional Independence Measure6-12 monthsPatient function as measured by Functional Independence Measure compared to platelet inhibition

Countries

United States

Outcome results

None listed

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