- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00213070
Double-Blind Trial of Miglitol in Type 2 Diabetic Patients With Insulin Treatment
September 20, 2006 updated by: Sanwa Kagaku Kenkyusho Co., Ltd.
The purpose of this study is evaluate the clinical efficacy and safety of Miglitol in patients with Type2 Diabetes Mellitus with treated insulin.
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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Gifu, Japan
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Gunma, Japan
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Hokkaido, Japan
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Ibaraki, Japan
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Kagoshima, Japan
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Kanagawa, Japan
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Kumamoto, Japan
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Miyazaki, Japan
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Oita, Japan
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Okinawa, Japan
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Saitama, Japan
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Shiga, Japan
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Tokyo, 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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Type2 diabetes
- Criteria of postprandial plasma glucose and HbA1c are met
Exclusion Criteria:
- Type1 diabetes
- Patients with antidiabetic drugs
- The other exclusion criteria are met
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 Assignment
- Masking: Double
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Clinical Promotion Group, Sanwa Kagaku Kenkyusho Co., Ltd.
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 13, 2005
First Submitted That Met QC Criteria
September 13, 2005
First Posted (Estimate)
September 21, 2005
Study Record Updates
Last Update Posted (Estimate)
September 21, 2006
Last Update Submitted That Met QC Criteria
September 20, 2006
Last Verified
September 1, 2006
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MG1005
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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