Clinical Study on Efficacy and Safety of Hetrombopag in the Preoperative Patients of Thrombocytopenia

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe Third People's Hospital of Chengdu

About this trial

This is an investigator-initiated, single-arm, prospective clinical study to evaluate the efficacy and safety of heptapopal in the treatment of thrombocytopenia prior to elective surgery

Eligibility criteria

Qualifiers

Age ≥18 years old; diagnosis of immune thrombocytopenia.

Platelets ≤75×10^9/L before scheduled elective surgery.

Disqualifiers

History of allergy to Thrombopoietin Receptor Agonists (TPO-RA) drugs;

Severe bleeding symptoms, such as gastrointestinal bleeding, bleeding of important organs, and intracranial bleeding;

Thrombotic diseases, such as pulmonary embolism, arterial thrombosis and disseminated intravascular coagulation (DIC);

Positive anti-human immunodeficiency virus antibody or anti-treponema pallidum specific antibody;

Trial design

Treatments tested in this trial

  • Hetrombopag

Treatment groups

55 Participants
are divided into 1 treatment group

Sponsors and collaborators

The Third People's Hospital of Chengdu

Lead sponsor

Affiliated Hospital of North Sichuan Medical College

Collaborator