UMIN ID: UMIN000001759
Registered date:01/07/2009
Double blind, randomized Placebo-controlled study for FD
Basic Information
Recruitment status | Complete: follow-up complete |
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Health condition(s) or Problem(s) studied | functional dyspepsia |
Date of first enrollment | 2010/06/01 |
Target sample size | 200 |
Countries of recruitment | Japan |
Study type | Interventional |
Intervention(s) | anti-secretory drug placebo |
Outcome(s)
Primary Outcome | Severity of dyspeptic symptoms by symptomatic scale and GSRS |
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Secondary Outcome | Patients' background anti-H. pylori IgG |
Key inclusion & exclusion criteria
Age minimum | 20years-old |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude criteria | Patients with organic disease |
Related Information
Primary Sponsor | Office of the ELF study |
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Secondary Sponsor | |
Source(s) of Monetary Support | Donation |
Secondary ID(s) |
Contact
public contact | |
Name | Naoki Tomotsugu, Ph.D. |
Address | 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan Japan |
Telephone | 03-5363-3288 |
naokit@sc.itc.keio.ac.jp | |
Affiliation | Keio University School of Medicine Center for Clinical Research |
scientific contact | |
Name | Hidekazu Suzuki, M.D., Ph.D. |
Address | 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan Japan |
Telephone | 03-5363-3914 |
Affiliation | Keio University School of Medicine Division of Gastroenterology and Hepatology, Department of Internal Medicine |