Efficacy of Galeo® in Patients With Postprandial Distress Syndrome Subtype in Functional Dyspepsia

NCT ID: NCT05199441

Last Updated: 2024-01-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 226 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-02-25
• Study Completion Date: 2023-07-07

Brief Summary

The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Galeo® on dyspepsia symptoms in patients with postprandial distress syndrome subtype in functional dyspepsia for 8 weeks.

Detailed Description

Galeo® already used an over-count drug for the improvement of dyspepsia symptoms. The investigators conduct a multi-center, double-blind, randomized, placebo-controlled, parallel-group study to investigate the effects of Galeo® on dyspepsia symptoms in patients with postprandial distress syndrome subtype in functional dyspepsia for 8 weeks; the safety of the compound is also evaluated. The Investigators examine gastrointestinal symptom score (GIS) score, the Korean version of Nepean dyspepsia index (K-NDI), and OV efficacy at baseline and after 8 weeks of intervention. A total of 226 subjects were administered either 1,500 mg of Galeo® or a placebo each day for 8 weeks.

Conditions

Dyspepsia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Dihydroxydibutylether group

This group takes dihydroxydibutylether for 8 weeks.

Group Type: EXPERIMENTAL

Dihydroxydibutylether group

Intervention Type: DRUG

This group takes 1.500 mg/day of dihydroxydibutylether for 8 weeks.

Control group

This group takes placebo for 8 weeks.

Group Type: PLACEBO_COMPARATOR

Control group placebo

Intervention Type: DRUG

This group takes 1,500 mg/day of placebo for 8 weeks.

Interventions

Dihydroxydibutylether group

This group takes 1.500 mg/day of dihydroxydibutylether for 8 weeks.

Intervention Type: DRUG

Control group placebo

This group takes 1,500 mg/day of placebo for 8 weeks.

Intervention Type: DRUG

Other Intervention Names

Galeo® group; Placebo

Eligibility Criteria

Inclusion Criteria

• postprandial distress syndrome according to Rome III criteria
• Those who have at least 3 of the 10 symptoms of the GIS evaluation are moderate or more and have at least 1 of bloating, delayed digestion, belching, and nausea
• Those with no organic lesions on the upper gastrointestinal endoscopy within 3 months prior to screening

Exclusion Criteria

• Those who have confirmed the following medical history or surgical history at the time of screening

1. Surgery that may affect gastrointestinal motility (eg, laparoscopic or laparotomy of the gastrointestinal tract) (except for appendectomy and hysterectomy due to simple appendicitis)

2. Diseases that can cause organic dyspepsia, such as irritable bowel syndrome, inflammatory bowel disease, gastroesophageal disease, and duodenal disease (gastric ulcer, esophagitis [from RE A], etc.) within 3 months before screening history of drug use

3. Malignant tumors of the digestive system (except in cases where there is no history of recurrence within 5 years or cases where a cure has been obtained)

4. Other malignant tumors other than the digestive system within 5 years (however, except for if there is no history of recurrence within 5 years or cured cases)

5. History of organic neurological or psychiatric disorders (major depressive disorder or anxiety disorder, etc.), alcoholism, substance abuse, and drug dependence (except nicotine and caffeine)

• Those with the following diseases at the time of screening

1. Organic causes of gastroparesis (diabetic gastroparesis, etc.)

2. glaucoma

3. urinary tract disease or prostate disease

4. Biliary duct obstruction or biliary duct stones (eg, intrahepatic gallstones, extrahepatic gallstones)

5. uncontrolled diabetes mellitus (glycated hemoglobin > 8.0%)

6. Aspartate transaminase or alanine aminotransferase levels are more than 3 times the upper limit of normal, or total bilirubin levels are more than 3 times the upper limit of normal, or liver disease

7. Serum creatinine level is 1.5 times or more of the upper limit of normal, or renal disease

8. Other clinically significant diseases of the heart (blood pressure 160/100 mmHg or more), kidney, lung, blood, and endocrine system, and dysfunction that may affect efficacy and safety evaluation

• Those who have administered the following drugs that may affect efficacy evaluation within 2 weeks before screening

1. emollient: artichoke extract, ursodeoxycholic acid, etc.

2. prokinetics: metoclopramide, itopride, etc.

3. inhibitors of gastric acid secretion: H2 receptor antagonist (proton pump inhibitor), gastric acid pump antagonist (acid pump antagonist)

4. gastric mucosal protective agent, antacid, digestive agent

5. fundus relaxants: sumatriptan, buspirone, etc.

6. cholinergic, anticholinergic and antispasmodic

7. psychotropic drugs: antipsychotic drugs, antidepressants, antimanic drugs, antianxiety drugs, hallucinogens, etc.

8. Nonsteroidal anti-inflammatory drugs (intermittent administration up to 1 week 2 days and cyclooxygenase-2 selective inhibitors are acceptable)

9. Antithrombotic agents (antiplatelet agents, anticoagulants)

10. systemic glucocorticoids

11. Erythromycin (However, in the case of eye drops, the administration is allowed) If the above drugs are administered, registration is possible after a wash-out period of at least 2 weeks, and drugs used for the purpose of pretreatment for upper gastrointestinal endoscopy (midazolam, propofol, simethicone), hyoscine butylbromide, cimetropium bromide, etc.) are allowed within 1 day.

• Those who received Helicobacter pylori eradication treatment within 2 weeks before screening
• Those who have administered or treated other clinical trial drugs or medical devices within 3 months prior to screening
• Pregnant or lactating women
• Women or men of childbearing potential who are unwilling to use an appropriate method of contraception* during this clinical trial

*hormonal contraceptives, implantation of intrauterine devices or intrauterine systems, vasectomy, tubal ligation, double-blocking contraception (using a cervical cap or diaphragm and a male condom simultaneously), etc.

• If there are other diseases that may affect this clinical trial
• Persons with hypersensitivity or allergy to clinical investigational drugs and similar drugs or to soybean oil, soybean, peanut
• Persons judged unsuitable to participate in clinical trials by investigators

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pusan National University Yangsan Hospital

OTHER

Sponsor Role: lead

Responsible Party

Sang Yeoup Lee

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sang Yeoup Lee, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Pusan National University Yangsan Hospital

Locations

Pusan National University Yangsan Hospital

Yangsan, Gyeungsangnam-do, South Korea

Countries

South Korea

Other Identifiers

02-2021-034

Identifier Type: -

Identifier Source: org_study_id