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ENROLLING BY INVITATION
NCT06642740

Study on the Efficacy and Safety of Avatricopal in Patients With CLD Complicated With Thrombocytopenia

Sponsor: Beijing Ditan Hospital

View on ClinicalTrials.gov

Summary

In this study, patients with chronic liver disease undergoing selective invasive and minimally invasive surgery combined with thrombocytopenia were enrolled. After enrollment, liver disease treatment was supplemented with avatripopal for 5 days. Biochemical indexes of avatripopal were monitored during treatment and after withdrawal. The proportion of patients with platelet count ≥50×10\^9/L on the day of selective invasive and minimally invasive surgery was analyzed. The incidence of adverse events was observed.

Official title: Study on the Efficacy and Safety of Avatricopal in Patients With Chronic Liver Disease With Selective Invasive and Minimally Invasive Surgery Combined With Thrombocytopenia

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

69

Start Date

2024-06-01

Completion Date

2025-06-01

Last Updated

2024-10-15

Healthy Volunteers

No

Interventions

OTHER

Platelet count

divide into two groups based on platelet count

Locations (1)

Beijing Ditan Hospital,Capital Medical University

Beijing, Beijing Municipality, China