Reference Range Study for the Quantra System With the QPlus Cartridge in Pediatric Patients

Part of paid clinical trials in Los Angeles, California.

Sponsor
HemoSonics LLC
Study ID
NCT07447713
Status
Not Yet Recruiting

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Conditions

  • Coagulation
  • Pediatric

Eligibility Criteria

Sex
ALL
Age
N/A - 17 Years
Healthy Volunteers
Not accepted

Interventions

  • Quantra System — DIAGNOSTIC_TEST
    Diagnostic device to monitor coagulation properties of a whole blood sample at the point-of-care.

Study Details

This study will determine reference range intervals for the parameters reported by the Quantra System with the QPlus Cartridge in pediatric patients.

Key Dates

Start date
Apr 15, 2026
Status verified
Feb 2026
Primary completion
Apr 30, 2027
Completion
May 30, 2027

Study Design

Enrollment
240 participants (estimated)

Arms

  • Arm: Pediatric patients

Primary Outcome Measure

Reference range intervals for measurement of Clot Time (CT) parameter [ Time Frame: Baseline, determined from a single blood draw ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
UCLA Mattel Children's HospitalLos AngelesCalifornia90095
Department of Anesthesiology
Children's Healthcare of AtlantaAtlantaGeorgia30329
Department of Anesthesiology
Boston Children's HospitalBostonMassachusetts02115
Department of Anesthesiology

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