- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00380822
Double-Blind Study of Miglitol in Japanese With type2 Diabetes
September 25, 2006 updated by: Sanwa Kagaku Kenkyusho Co., Ltd.
To investigate the efficacy and safety of miglitol in Japanese patients with type 2 diabetes that is insufficiently controlled diet alone.
Study Overview
Study Type
Interventional
Phase
- Phase 3
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Aichi, Japan
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Chiba, Japan
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Fukuoka, Japan
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Gunma, Japan
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Hiroshima, Japan
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Hyogo, Japan
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Ibaragi, Japan
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Ishikawa, Japan
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Iwate, Japan
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Kumamoto, Japan
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Kyoto, Japan
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Mie, Japan
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Miyagi, Japan
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Nagasaki, Japan
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Niigata, Japan
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Oita, Japan
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Okayama, Japan
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Osaka, Japan
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Saga, Japan
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Saitama, Japan
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Shiga, Japan
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Shimane, Japan
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Shizuoka, Japan
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Tokyo, Japan
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Toyama, Japan
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Yamagata, Japan
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Yamaguchi, Japan
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 69 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Type2 diabetic patient on Dietary Therapy
- Criteria for postprandial plasma glucose and HbA1c are met
Exclusion Criteria:
- Type1 diabetes
- Patients treated with antidiabetic drugs or Insulin
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
September 25, 2006
First Submitted That Met QC Criteria
September 25, 2006
First Posted (ESTIMATE)
September 27, 2006
Study Record Updates
Last Update Posted (ESTIMATE)
September 27, 2006
Last Update Submitted That Met QC Criteria
September 25, 2006
Last Verified
September 1, 2006
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MG1001
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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