Efficacy and Safety of Repaglinide, Glurenorm® and Glucobay® in Chinese Subjects With Type 2 Diabetes
NCT ID: NCT00568074
Last Updated: 2017-02-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
131 participants
INTERVENTIONAL
2003-12-16
2004-09-02
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
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repaglinide
Glurenorm®
Glucobay®
Eligibility Criteria
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Inclusion Criteria
* No previous treatment for diabetes
* HbA1c: 7.0-12.0%
Exclusion Criteria
* Uncontrolled treated/untreated hypertension
* Any condition that the Investigator and/or Sponsor feels would interfere with trial participation or evaluation of results
* Pregnancy, breast-feeding, the intention of becoming pregnant or judged to be using inadequate contraceptive measures (adequate contraceptive measures are: sterilisation, intra-uterine device (IUD), oral contraceptives or barrier methods)
30 Years
ALL
No
Sponsors
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Novo Nordisk A/S
INDUSTRY
Responsible Party
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Principal Investigators
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Global Clinical Registry (GCR, 1452)
Role: STUDY_DIRECTOR
Novo Nordisk A/S
Locations
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Novo Nordisk Investigational Site
Shanghai, Shanghai Municipality, China
Novo Nordisk Investigational Site
Shanghai, Shanghai Municipality, China
Novo Nordisk Investigational Site
Chengdu, Sichuan, China
Novo Nordisk Investigational Site
Beijing, , China
Countries
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Related Links
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Clinical Trials at Novo Nordisk
Other Identifiers
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AGEE-1555
Identifier Type: -
Identifier Source: org_study_id
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