JRCT ID: jRCT2080220830
Registered date:26/08/2009
Basic Information
Recruitment status | |
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Health condition(s) or Problem(s) studied | Prevention of onset of low dose aspirin related gastric ulcer |
Date of first enrollment | 26/08/2009 |
Target sample size | |
Countries of recruitment | |
Study type | Interventional |
Intervention(s) | investigational material(s) Generic name etc : AG-1749 INN of investigational material : Therapeutic category code : 232 Agents for peptic ulcer Dosage and Administration for Investigational material : oral |
Outcome(s)
Primary Outcome | |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | >= 20age old |
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Age maximum | Not applicable |
Gender | Both |
Include criteria | 1. Patients who have finished the preceding confirmatory anti-ulcer efficacy study 2. Patients who are on oral low-dose aspirin at the time of consent and who require continued long-term use of low-dose aspirin even after the start of study treatment in this study |
Exclude criteria |
Related Information
Primary Sponsor | Takeda Pharmaceutical Company Limited |
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Secondary Sponsor | |
Source(s) of Monetary Support | |
Secondary ID(s) | JapicCTI-090861 |
Contact
Public contact | |
Name | |
Address | https://www.takeda.co.jp/contact/form/en/form/index.html |
Telephone | |
Affiliation | Takeda Pharmaceutical Company Limited |
Scientific contact | |
Name | |
Address | https://www.takeda.co.jp/contact/form/en/form/index.html |
Telephone | |
Affiliation | Takeda Pharmaceutical Company Limited |