Clinical Trial for the Evaluation of the Efficacy and Safety of EDL on Dyspepsia

Launched by SEOUL NATIONAL UNIVERSITY BUNDANG HOSPITAL · Jul 19, 2020

Keywords

ClinConnect Summary

This clinical trial is studying the effects of a natural extract called EDL (Extract of Dolichos lablab Linne) on adults who suffer from functional dyspepsia, a condition that causes discomfort in the upper stomach, including symptoms like feeling overly full after meals, pain, or burning sensations. The goal is to see if EDL can help improve these symptoms compared to a placebo, which is a harmless substance that looks like the treatment but has no active ingredients.

To join the trial, participants need to be at least 19 years old and have been diagnosed with functional dyspepsia. They should have experienced certain symptoms for at least six months, and tests must show that there are no underlying issues causing these symptoms. Those interested can expect to be part of a study that monitors their symptoms over time while taking the EDL or placebo. It's important to know that individuals with certain health conditions, recent surgeries, or who are taking specific medications may not be eligible to participate. If you're considering joining, you'll need to give your consent and sign a form before starting the trial.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Those over the age of 19
• • 2. Those diagnosed with functional dyspepsia (Rome IV\*)
• • \* One or more of the following symptoms are diagnosed when there is no organic cause in the test including the upper gastrointestinal endoscopy(if symptoms begin 6 months prior to Visit 1, and the symptoms are present in the past 3 months).
• • Othersome postprandial fullness
• • Unpleasant early satiation
• • Unpleasant epigastric pain
• • Unpleasant epigastric burning
• • 3. A person who has 4 or more of the 10 symptoms in the GIS (Gastrointestinal Symptom) questionnaire and has a total score of 12 or more (5-point Likert scale)
• • 4. When there is no organic disease in the gastroscopy performed at Visit 1 (however, it can be replaced by the test results within 3 months from Visit 1)
• • 5. A person who consented to participate in this clinical trial and signed a Informed consent form before the trail began.
• Exclusion Criteria:
• • 1. Persons who are currently being treated with severe cardiovascular system, immune system, respiratory system, hepatobiliary system, kidney and urinary system, nervous system, musculoskeletal system, mental, infectious diseases, and malignant tumors (however, considering the condition of the subjects, subjects can participate in the test according to investigator's judgment.)
• • 2. Persons with a history of peptic ulcer and reflux esophagitis within 6 months of Visit 1
• • 3. Those who have gastrointestinal surgery (except appendectomy and hemorrhoidectomy)
• • 4. Persons with a history of malignancy of the digestive system
• • 5. Those who have taken H2 receptor blockers, anticholinergic agents (muscarinic receptor antagonists), gastrin receptor antagonists, prostaglandin preparations, proton pump inhibitors, gastric mucosal protective agents, other drugs intended to treat gastritis, gastric health-related health functional food within 2 weeks of Visit 1
• • 6. Those who need to constantly take medications that can cause gastritis, such as adrenal cortical hormones, nonsteroidal anti-inflammatory drugs, and aspirin during the human application test {However, low-dose aspirin for cardiovascular disease prevention (100 mg/day or less) permit}
• • 7. In the Drinking Habit Questionnaire, those who had an average alcohol intake of 14 units or more for men and or more 7 units for women per week for the past month.
• • 8. Uncontrolled hypertension persons (systolic blood pressure of 160 mmHg or higher, or diastolic blood pressure of 100 mmHg or higher, measurement criteria after 10 minutes of stability in human subjects)
• • 9. Persons with uncontrolled diabetes (fasting blood sugar is over 180 mg/dL)
• • 10. Those whose Creatinine is more than twice the normal upper limit of the study institution
• • 11. Those whose AST(GOT) or ALT(GPT) is more than 3 times the normal upper limit of the study institution
• • 12. Persons who are sensitive or allergic to investigational product for this clinical trial
• • 13. Pregnant, lactating or planning to become pregnant within 3 months
• • 14. Those who participated in other clinical trials within 3 months of Visit 1 or plan to participate in other clinical trials after the start of this clinical trials.
• • 15. A person who determines that the Investigator is inappropriate for clinical trials
• • 16. Employee of Department of Digestive Internal Medicine, Seoul National University Bundang Hospital