Actively Recruiting
Primary Care dySpEpsia rikkuNshiTo
Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2025-07-23
100
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Dyspepsia refers to chronic or recurrent upper gastrointestinal (GI) symptoms originating from the gastroduodenal region with a significant impact on patients' lives. Functional dyspepsia comprises the diagnostic categories of epigastric pain syndrome (EPS) with epigastric pain or burning and postprandial distress syndrome (PDS) with meal-related fullness or early satiation, which are unexplained after routine investigation including upper GI endoscopy 2. Despite the common occurrence of FD in up to 15% of the general population, the underlying pathophysiology remains unclear and no treatments of proven efficacy are available in Europe for this condition. Our group has demonstrated increased duodenal mucosal permeability and low-grade inflammation in FD patients, correlating with meal-related symptoms. The causes of the barrier defect and immune activation are unknown but candidates include psychological stress, luminal food components, (bile) acid and microbiota. The symptoms most closely associated with increased eosinophil counts in the duodenum are early satiation and postprandial fullness, which are typical PDS symptoms, and which are also associated with impaired gastric accommodation to meal ingestion and delayed gastric emptying. Previously the efficacy of the Kampo medicine Rikkunshito (TJ-43) has been shown in FD. The exact mode of action remains to be determined. Previous studies have provided mechanistic evidence that rikkunshito is able to improve gastric accommodation, improve food intake and enhance circulating levels of the orexigenic gut peptide ghrelin. The aim of this study is to evaluate the efficacy of Rikkunshito in comparison to placebo in PDS patients recruited from primary care in Belgium, and to evaluate whether this is associated with changes in duodenal mucosal low-grade inflammation.
CONDITIONS
Official Title
Primary Care dySpEpsia rikkuNshiTo
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Voluntary written informed consent obtained before screening
- Use of highly effective birth control methods if applicable
- Male or female participants
- 18 years old or older
- Newly diagnosed with functional dyspepsia
- Able to understand and comply with study requirements
You will not qualify if you...
- History of type 1 or type 2 diabetes, eosinophilic esophagitis, celiac disease, inflammatory bowel disease, or major abdominal surgery (except appendectomy, cholecystectomy, or splenectomy)
- Any disorder that may jeopardize participant safety or protocol compliance as judged by the investigator
- Prior or current treatments that could affect safety or trial integrity
- Pregnant, breastfeeding, or intending to become pregnant females not using effective contraception
- Predominant symptoms of gastroesophageal reflux disease or irritable bowel syndrome
- Active somatic or psychiatric conditions explaining dyspeptic symptoms or severe depression (PHQ-7 score 20-27)
- Current or recent (within 2 weeks) proton pump inhibitor therapy
- Active malignancy
- Known HIV, HBV, or HCV infection
- Significant alcohol use (more than 10 units per week)
- Known allergy to Rikkunshito or its ingredients
- Overweight with BMI greater than 26
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
KU Leuven
Leuven, Vlaams-Brabant, Belgium, 3000
Actively Recruiting
Research Team
J
Jan Tack, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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