This study is a prospective, randomized, parallel-controlled clinical trial. The primary objective is to evaluate the superiority and safety of nanocrystalline megestrol acetate in combination with standard therapy compared with standard therapy alone in improving appetite and body mass index (BMI) during treatment in patients with early-stage or locally advanced hepatocellular carcinoma at the cachexia stage.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
68
Nanocrystalline Megestrol Acetate oral suspension, with a specification of 125 mg/mL, administered orally at a dose of 5 mL per day (625 mg/day), and the primary endpoint efficacy collection will be conducted in the 4th week.
Standard Antitumor Therapy
West China School of Medicine/West China Hospital of Sichuan University
Chengdu, Sichuan, China
The proportion of subjects with improved appetite based on A/CS-12 assessment.
Time frame: The proportion of subjects with improved appetite based on A/CS-12 assessment in 12 weeks
Proportion of patients with BMI increase
Time frame: Proportion of patients with BMI increase in 12 weeks
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