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Healing Effects of Rebamipide and Omeprazole in Helicobacter Pylori-positive Gastric Ulcer After Eradication Therapy

A Comparative Study on the Healing Effects of Rebamipide and Omeprazole in Helicobacter Pylori-positive Gastric Ulcer After Eradication Therapy

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00272467
Enrollment
132
Registered
2006-01-06
Start date
2005-07-31
Completion date
2008-04-30
Last updated
2015-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stomach Ulcer

Keywords

Helicobacter pylori, Stomach ulcer, Rebamipide, Omeprazole

Brief summary

The purpose of this study is to evaluate the ulcer healing efficacy of rebamipide in comparison with omeprazole in Helicobacter pylori-positive gastric ulcer after eradication therapy.

Detailed description

This study is designed to evaluate the ulcer healing efficacy of rebamipide administered following the eradication therapy in comparison with the well known PPI, omeprazole. This is a double-blind, comparative study which is expected to prove the role of rebamipide in gastric ulcer healing after the eradication therapy. This study may contribute to further clinical research on a new type of ulcer treatment by looking at the treatment modality based on the enhancement of defensive factors.

Interventions

DRUGRebamipide

1. Brand name: Mucosta® Tab. 2. Generic name: Rebamipide. 3. Chemical name: (±)-2-(4-chlorobenzoylamino)-3-\[2(1H)-quinolinon-4-yl\]propionic acid. 4. Formulation: Tablet (White, film-coated tablet). 5. Strength: One tablet contains rebamipide 100mg. 6. Storage condition: 15℃\ 25℃. 7. Manufacturer: Korea Otsuka Pharmaceuticals

DRUGOmeprazole

1. Brand name: Losec® Cap. 2. Generic name: Omeprazole. 3. Chemical name: 5-melthoxy-2-{{{4-melthoxy-3.5-dlmethyl2-pyridinyl}methyl}sulp- hinyl}-1H-benzimidazole sodium. 4) Formulation: Capsule. 5) Strength: One capsule contains omeprazole 20mg. 6) Storage condition: 15℃\ 25℃. 7) Manufacturer: AstraZenaca Korea.

Sponsors

Zhejiang Otsuka Pharmaceutical Co., Ltd.
CollaboratorINDUSTRY
Korea Otsuka Pharmaceutical Co., Ltd.
CollaboratorINDUSTRY
Korea Otsuka International Asia Arab
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 20 or older at the time of writing the informed consent * H. pylori-positive patient. * Patients who are diagnosed with gastric ulcer by endoscopy and have the following ulcer characteristics; Non-scarring ulcer (stage A1, A2, H1, H2 according to the Sakita-Miwa classification), Single ulcer, Ulcer size of 5 to 20mm in diameter

Exclusion criteria

* Patients who previously underwent H. pylori eradication therapy * Malignant gastric ulcer * Linear ulcer * Patients with history of upper GI tract resection or vagotomy * Patients with continuous NSAIDs use within 4 weeks prior to study initiation * Patients with ulcer complications including perforation or pyloric stenosis * Gastric ulcer prone to bleeding (e.g. exposed blood vessels at ulcer base) * Patients with infectious mononucleosis * Patients with known hypersensitivity to penicillin, clarithromycin, omeprazole, amoxicillin or rebamipide * Patients on medications such as terfenadine or pimozide which are contraindicated with clarithromycin usage * Pregnant or possibly pregnant women, lactating women, or those with a plan to conceive during this study * Blood test results of Hb ≤ 8.0 g/dl, platelet ≤50,000 /㎕, total WBC ≤ 4000/㎕ or ≥ 10,000/㎕, and with serum test results showing the levels of AST, ALT, ALP, LDH, BUN, and creatinine exceeding twice the normal range of respective institution. * Other patients deemed not eligible for this study by investigators

Design outcomes

Primary

MeasureTime frameDescription
Gastric ulcer healing rateat 12 weeks after the initial administration of the study medicationRebamipide showed 81.5\ 87.8% of gastric ulcer healing rate which was not inferior to 82.5\ 87.8% healing rate of Omeprazole.

Secondary

MeasureTime frameDescription
Gastric ulcer healing rate in cases with successful H.pylori eradication and H.pylori eradication failure (12 weeks after administration of the study medication.)at 12 weeks after the initial administration of the study medication
Serum gastrin levelat 8 and 12 weeks after the initial administration of study medication
Economical efficiencydrug cost/effect ratioRebamipide was more cost effective than Omeparzole for 7 weeks of gastric ulcer treatment.

Countries

China, South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026