Summary

Eligibility
for people ages up to 18 years (full criteria)
Location
at UCLA
Dates
study started
study ends around

Description

Summary

This study will evaluate the performance of the Quantra System with the QPlus Cartridge in pediatric patients undergoing cardiovascular procedures.

Official Title

Evaluation of the Clinical Performance of the Quantra System With the QPlus Cartridge in Pediatric Patients Undergoing Cardiovascular Procedures

Details

Pediatric patients that require major sugical procedures, such as cardiac surgery, are especially vulnerable to perioperative coagulopathy due to age-related immaturity of the hemostatic system, exposure to hemodilution from circuit primes or intravenous volume loading, hypothermia during complex interventions, and the intrinsic bleeding of invasive cardiac procedures. These factors can produce clinically significant perioperative bleeding driven by platelet dysfunction, hypofibrinogenemia and other hemostatic defects. The Quantra System with the QPlus Cartridge is desinged to assess coagulation function of a whole blood sample at the point-of-care by measuring changes in the viscoelastic properties during clot formation. This multi-center study is aimed to demonstrate the performance of the QPlus Cartridge for its ability to aid in the evaluation of a pediatric patient's hemostatic status before, during and after cardiovascular procedures.

Keywords

Blood Loss, Surgical, Viscoelastic testing, Quantra, QPlus Cartridge, Pediatric, Cardiovascular surgery, Surgical Blood Loss, Quantra System

Eligibility

You can join if…

Open to people ages up to 18 years

  • Subject is <18 years of age.
  • Subject is undergoing a cardiovascular procedure OR subject underwent cardiovascular surgery and presents with acute bleeding or suspected hypocoagulation/hypercoagulation in a post-surgical unit.
  • Subject's parent(s) or guardian(s) has signed an informed consent form. If required, subject has signed an assent form.

You CAN'T join if...

  • Corrected gestational age <37 weeks.
  • Subject is enrolled in a study that might confound the result of the proposed study.
  • Subject is affected by a condition that, in the opinion of the clinical team, may pose additional risks.

Locations

  • UCLA Mattel Children's Hospital
    Los Angeles California 90095 United States
  • Children's Healthcare of Atlanta
    Atlanta Georgia 30329 United States
  • Children's Hospital of Philadelphia
    Philadelphia Pennsylvania 19104 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
HemoSonics LLC
ID
NCT07597278
Study Type
Observational
Participants
Expecting 160 study participants
Last Updated