Clinical Trial

A Prospective Multicentre Real-world Assessment of the Efficacy of Danning Tablets in Alleviating Digestive Symptoms

Recruiting
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Summary
The goal of this observational study is to evaluate if Danning Tablets are effective in alleviating dyspepsia in patients with any of the following digestive symptoms: upper abdominal pain, bloating, loss of appetite, acid reflux or constipation. The main questions it aims to answer are: How effective are Danning Tablets for patients with indigestion symptoms? What are the impact factors (e.g. severity of conditions, demographic features, dose and length of treatment etc.) of the efficacy of Danning Tablets for indigestion patients? Participants already taking Danning Tablets as part of their regular medical care for indigestion will take questionnaires by the end of two weeks and four weeks respectively from the start of their treatment.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-12-24.
Status change: Not Yet Recruiting → Recruiting 2025-05-13
Trial Details
NCT Number NCT06755671
Lead Sponsor Shanghai Hutchison Pharmaceuticals Limited
Collaborators: Second Affiliated Hospital, Zhejiang University, School of Medicine
Conditions Indigestion, Dyspepsia, Bloating, Loss of Appetite, Reflux Acid, Constipation, Upper Abdominal Pain, Functional Dyspepsia
Enrollment 4,500 participants
Start Date 2025-04-30
Primary Completion 2027-06-30 (estimated)
Study Completion 2027-06-30 (estimated)
Updated on ClinicalTrials.gov 2025-05-14