Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT06482671

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

KU Leuven

Leuven, Vlaams-Brabant, Belgium, 3000

Actively Recruiting

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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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