drugset / Trial / NCT04380233

Zhizhu Kuanzhong Capsule for Patients With Functional Dyspepsia-Postprandial Distress Syndrome

NCT04380233 ↗

RandomizedParallel-groupTriple-blindTreatment

Summary

A 13 weeks randomized, double-blind and placebo parallel-controlled trial will be conducted to evaluate the clinical efficacy and safety of Zhizhu Kuanzhong Capsule in the treatment of functional dyspepsia-postprandial distress syndrome.

Timeline

Start
2021-04-01
Primary completion
2022-02-28
Completion
2022-03-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Zhizhu Kuanzhong Capsule Traditional medicine (herbal / TCM) 1.29 g Oral

Indications