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GlucoFriend-evaluation the Effectiveness of Glucobay When Combined With a Basal Insulin

Information source: Bayer
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Diabetes Mellitus

Intervention: Acarbose (Glucobay, BAYG5421) (Drug)

Phase: N/A

Status: Completed

Sponsored by: Bayer

Official(s) and/or principal investigator(s):
Bayer Study Director, Study Director, Affiliation: Bayer

Summary

To evaluate the effectiveness of Glucobay when combined with a basal insulin under daily-life treatment conditions in a large sample of Korean patients.

Clinical Details

Official title: Combined Use of a Basal Insulin and Glucobay For Reducing PPG to End Diabetes Progress

Study design: Time Perspective: Prospective

Primary outcome: Change in HbA1c

Secondary outcome:

Duration and dose of acarbose treatment

Postprandial Blood Glucose

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Signed written informed consent

- Age ≥ 18 years

- Diagnosed of type 2 diabetes for at least 6 months prior to enrollment

- Patients treated with stable dose of a basal insulin (insulin glargine or insulin

detemir) at least 2 months

- HbA1C≥7. 5 and ≤10. 0%

Exclusion Criteria:

- Exclusion criteria must be read in conjunction with the local product information

Locations and Contacts

Many Locations, Korea, Republic of
Additional Information

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Starting date: September 2010
Last updated: June 19, 2013

Page last updated: August 23, 2015

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