Clinical Trials Directory

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UnknownNCT04946929

Ticagrelor in Post-transplant Patients With Pediatric Hepatic Artery Thrombosis (HAT)

Determine the Safety/Efficacy of Ticagrelor in Post-transplant Patients With Hepatic Artery Thrombosis (HAT)

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
RenJi Hospital · Academic / Other
Sex
All
Age
2 Months – 5 Years
Healthy volunteers
Not accepted

Summary

Hepatic artery thrombosis (HAT) represents a major cause of graft loss and mortality after Pediatric liver transplantation. Ticagrelor (a new reversible inhibitor of P2Y12 receptor with faster onset of action and greater platelet inhibition) was used to treat patients with pediatric post-transplant hepatic artery thrombosis (HAT) compared to low molecular weight heparin.

Detailed description

In pediatric patients with post-transplant hepatic artery thrombosis (HAT) , low molecular weight heparin is a commonly used method. Ticagrelor, a direct-acting and reversible ADP receptor antagonist, is now the most commonly used ADP receptor antagonist in the treatment of coronary diseases. Compared to its predecessor clopidogrel, the pharmacokinetic profil of ticagrelor is more predictable, demonstrating a faster onset of action and a more consistent platelet inhibition. However, because of the excellent antithrombotic effect and increased bleeding potential, it is recommended that major bleeding, such as OPCAB or CABG surgery, be expected with a high probability, and in case of fatal surgery, the drug should be discontinued for 5 days. The present study is to evaluate the safety and efficacy of Ticagrelor in pediatirc receipt with post-operative HAT.

Conditions

Interventions

TypeNameDescription
DRUGTicagrelor Oral Tablet [Brilinta]Ticagrelor, 2-3mg/kg, 12h, p.o.
DRUGLow molecular weight heparinhalf amount low molecular weight heparin

Timeline

Start date
2021-07-31
Primary completion
2022-12-31
Completion
2023-03-31
First posted
2021-07-01
Last updated
2021-07-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04946929. Inclusion in this directory is not an endorsement.