Status:
ENROLLING_BY_INVITATION
To Observe the Clinical Efficacy of Traditional Chinese Medicine Compound(Weipi Formula ) in the Treatment of Epigastric Stuffiness Syndrome
Lead Sponsor:
Second Affiliated Hospital of Nanchang University
Conditions:
Functional Dyspepsia(FD) Was Studied
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
The purpose of this clinical trial is to evaluate the efficacy of the herbal drug Weipi formula in treating functional dyspepsia (FD) in adults. It will also assess the safety of Weipi formula. The ma...
Eligibility Criteria
Inclusion
- ① Meet the diagnostic criteria for epigastric fullness (Pi-Man) in Traditional Chinese Medicine (TCM);
- Meet the Western diagnostic criteria for functional dyspepsia (FD), specifically postprandial distress syndrome (PDS) subtype, or meet both PDS and epigastric pain syndrome (EPS) subtypes but with PDS as the dominant presentation;
- Age 18-80 years;
- Willing to sign the informed consent form.
Exclusion
- ① Gastroscopy findings: Benign or malignant digestive diseases (e.g., peptic ulcer, gastric cancer);
- Severe organic diseases of the liver, gallbladder, spleen, or pancreas;
- Severe organic diseases in other organ systems;
- Pregnant or lactating women; ⑤ Patients with psychiatric disorders causing similar symptoms (e.g., schizophrenia, anxiety disorder, major depressive disorder); ⑥ Regular use (≥3 months) of NSAIDs and/or selective COX-2 inhibitors; ⑦ Potassium supplements taken within 2 weeks prior to enrollment.
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2026
Estimated Enrollment :
256 Patients enrolled
Trial Details
Trial ID
NCT06985524
Start Date
January 1 2024
End Date
December 31 2026
Last Update
May 22 2025
Active Locations (1)
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1
he Second Affiliated Hospital of Nanchang University, No. 1 Minde Road, Donghu District, Nanchang City, Jiangxi Province, China
Nanchang, Jiangxi, China, 330006