Actively Recruiting

Phase Not Applicable
Age: 19Years - 70Years
All Genders
Healthy Volunteers
NCT06630455

Meu-cinn for Gastric Mucosal Health in Adults With Functional Dyspepsia

Led by Pusan National University Yangsan Hospital · Updated on 2025-06-03

100

Participants Needed

1

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial aims to determine whether Meu-cinn promotes gastric mucosal health in adults with functional dyspepsia and to assess its safety. The main questions are: * Does Meu-cinn promote gastric mucosal health in participants? * What side effects occur when participants take Meu-cinn?

CONDITIONS

Official Title

Meu-cinn for Gastric Mucosal Health in Adults With Functional Dyspepsia

Who Can Participate

Age: 19Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 19 to 70 years
  • Diagnosed with functional dyspepsia based on Rome IV criteria
Not Eligible

You will not qualify if you...

  • Patients needing immediate drug treatment for gastrointestinal symptoms
  • History of hypersecretory gastric disorders like Zollinger-Ellison syndrome
  • Received Helicobacter pylori eradication therapy within 4 weeks before the study
  • Taken NSAIDs, steroids, antibiotics, aspirin, antithrombotic agents, or acid suppressants within the last month
  • History of upper gastrointestinal surgery, stricture, bleeding, or procedures like esophageal dilation or mucosal resection in the last year
  • Presence of active or healing gastric or duodenal ulcers, reflux esophagitis (LA grade A or higher), or malignant tumors found by endoscopy within the last 6 months
  • Uncontrolled hypertension (resting BP ≥160/100 mmHg)
  • Uncontrolled diabetes (fasting glucose ≥160 mg/dL)
  • Creatinine levels ≥ 2 times the upper limit of normal
  • Elevated liver enzymes (AST or ALT ≥ 2 times the upper limit of normal)
  • Alcohol abuse
  • Taking medications for psychiatric disorders (except intermittent sleep disorder medication)
  • Pregnant or breastfeeding women or planning pregnancy during the trial
  • Allergies to any components of the study foods
  • Participated or plans to participate in another drug clinical trial within the last month
  • Any other reason deemed unsuitable by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Pusan National University Yangsan Hospital

Yangsan, South Korea, 50612

Actively Recruiting

Loading map...

Research Team

S

Sang Yeoup Lee, Professor, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here