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RECRUITING
NCT06562738
PHASE4

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

Sponsor: The Third People's Hospital of Chengdu

View on ClinicalTrials.gov

Summary

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

55

Start Date

2024-06-01

Completion Date

2025-03-31

Last Updated

2024-08-20

Healthy Volunteers

No

Interventions

DRUG

Hetrombopag

Hetrombopag 7.5 mg, once a day, at bedtime for up to 14 days, drug administration was stopped when PLT≥100 ×10\^9/L, and take blood routine examination weekly, drug administration was resumed when PLT \< 100 ×10\^9/L. When PLT ≤30× 10\^9/L or ≥300 ×10\^9/L, take blood routine examination every 3 days.

Locations (1)

Chengdu Third People's Hospital

Chengdu, Sichuan, China