Platelet Transfusion and Repeat TEG-PM in Patients With Severe TBI on Antiplatelet Therapy (Repeat TEG-PM)

Part of paid clinical trials in Lancaster, Pennsylvania.

Sponsor
Lancaster General Hospital
Study ID
NCT06433622
Status
Enrolling By Invitation

Conditions

  • Traumatic Intracranial Hemorrhage

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Repeat Thromboelastography with Platelet Mapping — DIAGNOSTIC_TEST
    Thromboelastography (TEG) is an assay used by many medical professionals to assess coagulopathy, predict outcomes, and guide treatment. Although TEG does not assess platelet function very well, a TEG with platelet mapping (TEG-PM) assay assesses platelet functioning by measuring the percent of arachidonic acid (AA) and adenosine diphosphate (ADP) that are inhibited in the patient's blood.

Study Details

The aim of this study is to see if administering platelets (cells in our blood that stop or prevent bleeding) results in improved platelet function and slows/stops the progression of a head bleed for patients who have a traumatic head bleed and are on antiplatelet therapy (medications that stop blood cells from forming a blood clot) prior to admission.

Key Dates

Start date
Dec 1, 2023
Status verified
Oct 2025
Primary completion
Dec 31, 2026
Completion
Nov 30, 2027

Study Design

Enrollment
225 participants (estimated)

Arms

  • Arm: Repeat TEG-PM
    Will receive a repeat TEG-PM after platelet transfusion based on inclusion criteria.
  • Arm: No Repeat TEG-PM
    Not eligible to be consented; will proceed with normal course of treatment.

Primary Outcome Measure

Repeat TEG [ Time Frame: 1 hour after platelets given ]

Locations (1)

FacilityCityStateZIPSite coordinators
Penn Medicine Lancaster General HealthLancasterPennsylvania17602-

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