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| Tracking Information | |||||||||||||
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| First Received Date ICMJE | January 23, 2006 | ||||||||||||
| Last Updated Date | January 26, 2006 | ||||||||||||
| Start Date ICMJE | January 2006 | ||||||||||||
| Primary Completion Date | |||||||||||||
| Current Primary Outcome Measures ICMJE |
The effect of FP-01 on the eradication rates of H. pylori infection by a triple therapy | ||||||||||||
| Original Primary Outcome Measures ICMJE |
The effect of FP-01 on the eradication rates of H. pylori infection by atriple therapy | ||||||||||||
| Change History | Complete list of historical versions of study NCT00281047 on ClinicalTrials.gov Archive Site | ||||||||||||
| Current Secondary Outcome Measures ICMJE |
The effect o FP-10 on the eradication rates of clarithromycin-sensitive and -resistant strains of H. pylori by a triple therapy | ||||||||||||
| Original Secondary Outcome Measures ICMJE |
The effect o FP-10 on the eradication rates of clarithromycin-sensitive and -resistant strains of H. pylori by a triple tehrapy | ||||||||||||
| Descriptive Information | |||||||||||||
| Brief Title ICMJE | The Influence of FP-10 on the Eradication Rates of H. Pylori by a Triple Therapy | ||||||||||||
| Official Title ICMJE | The Phase 2 Study of FP-10, the Food Ingredient Derived From Milk Casein, on the Eradication Rates of Helicobacter Pylori by a Triple Therapy With Lansoprazole, Amoxicillin, and Clarithromycin | ||||||||||||
| Brief Summary | FP-10 is a food ingredient derived from milk casein. FP-10 can inhibit H. pylori to attach to the gastric epithelium. FP-10 has been made clear to decrease the intragastric urease activity (which is assumed to be produced by H. pylori) measured by the urea breath test. FP-10 can also detach H. pylori from gastric epithelium. We have hypothesized that FP-10 increases the eradication rates by a triple therapy with a proton pump inhibitor, amoxicillin, and clarithromycin. |
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| Detailed Description | H. pylori -positive patients older than 15 years of age with gastritis, gastric ulcer, duodenal ulcer, or gastroduodenal ulcer are invited to participate in the study. These patients had endoscopically and histologically proven ulcers or active chronic gastritis and are all H. pylori-positive. Written informed consent to participation must be obtained from each patient before the study. During gastroduodenoscopy, biopsy specimens obtained from both the antrum and the corpus of the greater curvature are subjected to the bacterial susceptibility to clarithromycin by culture test or measurements of 23S rRNA mutations at positions 2142 and 2143 (from adenine to guanine). Patients are treated with 30 mg of lansoprazole bid, 200 mg of clarithromycin bid, and 750 mg of amoxicillin bid for one week. In addition, they take placebo bid, FP10 1 g bid, or FP-10 2 g bid (2 hour after breakfast and at the bed time) for the same one week. Administration of placebo, FP-10 1 g or FP-10 2 g are performed in a double blinded manner. Eradication of H. pylori was confirmed by a 13C-urea breath test performed one month after eradication therapy. Throughout the study period, the investigators involved in the assessment of H. pylori eradication are blinded to susceptibility to clarithromycin H. pylori strains. |
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| Study Phase | Phase II, Phase III | ||||||||||||
| Study Type ICMJE | Interventional | ||||||||||||
| Study Design ICMJE | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study | ||||||||||||
| Condition ICMJE | Helicobacter Pylori | ||||||||||||
| Intervention ICMJE | Drug: FP-10 | ||||||||||||
| Study Arms / Comparison Groups | |||||||||||||
| Publications * |
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||||||||||
| Recruitment Status ICMJE | Recruiting | ||||||||||||
| Enrollment ICMJE | 138 | ||||||||||||
| Completion Date | May 2006 | ||||||||||||
| Primary Completion Date | |||||||||||||
| Eligibility Criteria ICMJE | Inclusion Criteria: H. pylori-positive patients who have never undergo the H. pylori eradication therapy - Exclusion Criteria: Patients not infected with H. pylori, Patients who are allergic to amoxicillin, clarithromycin, lansoprazole, 13C-urea, or milk casein - |
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| Gender | Both | ||||||||||||
| Ages | 15 Years to 90 Years | ||||||||||||
| Accepts Healthy Volunteers | No | ||||||||||||
| Contacts ICMJE |
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| Location Countries ICMJE | Japan | ||||||||||||
| Administrative Information | |||||||||||||
| NCT ID ICMJE | NCT00281047 | ||||||||||||
| Responsible Party | |||||||||||||
| Study ID Numbers ICMJE | Hp.FP-10.01 | ||||||||||||
| Study Sponsor ICMJE | Hamamatsu University | ||||||||||||
| Collaborators ICMJE | Oita University | ||||||||||||
| Investigators ICMJE |
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| Information Provided By | Hamamatsu University | ||||||||||||
| Verification Date | January 2006 | ||||||||||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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