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Spots Global Cancer Trial Database for Efficacy and Safety of Herombopag in Patients With Thrombocytopenia Before Hepatectomy

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Trial Identification

Brief Title: Efficacy and Safety of Herombopag in Patients With Thrombocytopenia Before Hepatectomy

Official Title: Director, Department of Liver Surgery, Fudan University Shanghai Cancer Center

Study ID: NCT05442632

Conditions

Hepatopathy

Interventions

Hetrombopag
Placebo

Study Description

Brief Summary: This is a single center, randomized, controlled study, to evaluate the efficacy and safety of Herombopag in patients with Thrombocytopenia before hepatectomy.

Detailed Description: The purpose of this study is to assess the ability of Herombopag to elevate platelet counts thereby reducing the need for platelet transfusions in patients with thrombocytopenia before hepatectomy. The clinical benefit of Herombopag will be measured by the proportion of subjects who avoid platelet transfusions, before, during and up to 7 days after undergoing an hepatectomy. In addition, bleeding events will be monitored during this time. The number of transfusions, safety events will be monitored during this time and for up to 3 months after undergoing a hepatectomy to help further evaluate clinical benefit.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Fudan University Shanghai Cancer Center, Shanghai, , China

Contact Details

Name: Lu Wang, Professor

Affiliation: Fudan University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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