← Back to Clinical Trials
Recruiting Phase 2 NCT06673498

NCT06673498 Lusutrombopag Combined With Recombinant Human Thrombopoietin for the Treatment of Thrombocytopenia in Patients With Chronic Liver Disease Destined to Undergo Elective Invasive Surgery

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT06673498
Status Recruiting
Phase Phase 2
Sponsor Anhui Provincial Hospital
Condition Thrombocytopenia
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2024-11-10
Primary Completion 2025-11-30

Trial Parameters

Condition Thrombocytopenia
Sponsor Anhui Provincial Hospital
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 60
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-11-10
Completion 2025-11-30
Interventions
Lusutrombopag combined with recombinant human thrombopoietin

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

Brief Summary

To assess the efficacy and safety of lusutrombopag combined with recombinant human thrombopoietin for the treatment of thrombocytopenia in patients with chronic liver disease destined to undergo elective invasive surgery.

Eligibility Criteria

Inclusion Criteria: * Ability to understand the study and willingness to comply with all study procedures by voluntarily signing an informed consent form prior to screening. * Male or female, 18 years of age or older at the time of signing the informed consent form. * Patients with chronic liver disease. * Baseline platelet count ≤ 35 x 109/L prior to enrolment on day 1. * Proposed elective invasive surgery that meets the following conditions: - Platelet transfusion may be required - Expected to be performed between days 9 and 15 after enrolment - Excludes extremely high-risk surgical operations such as open abdomen, open chest, open skull, and direct cardiac surgery. * Eastern Collaborative Oncology Group (ECOG) Physical Status (PS) score of 0 or 1. * According to the researcher, it will be able to fulfil the requirements of this study. * Male patients who are infertile or who agree to use adequate contraception (including the use of condoms containing spermicides) from the start of s

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology