Diabetes Mellitus Clinical Trial
Official title:
Diabetes Treatment by Glucobay® With a Special Therapeutic View to Chosen Patient Groups
Verified date | June 2023 |
Source | Bayer |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Evaluation of safety and effectiveness of Glucobay® under daily-life treatment conditions in a large sample of patients.
Status | Completed |
Enrollment | 15729 |
Est. completion date | December 31, 2010 |
Est. primary completion date | December 31, 2010 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patients with untreated or pretreated diabetes mellitus or patients for which acarbose is indicated and without acarbose treatment within the last three months before study inclusion. The decision for treatment type and duration is taken by the investigator and is made before inclusion into the study. Exclusion Criteria: - Exclusion criteria must be read in conjunction with the local product information. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Bayer |
Algeria, Bosnia and Herzegovina, Cambodia, China, Hong Kong, India, Indonesia, Korea, Republic of, Malaysia, Moldova, Republic of, Pakistan, Philippines, Russian Federation, Singapore, Thailand, Vietnam,
Zhang W, Kim D, Philip E, Miyan Z, Barykina I, Schmidt B, Stein H; Gluco VIP study. A multinational, observational study to investigate the efficacy, safety and tolerability of acarbose as add-on or monotherapy in a range of patients: the Gluco VIP study. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Data collection on patients weight and waist circumference, fasting blood glucose, postprandial blood glucose (2h), HbA1C; exploratory analysis according to patient groups (concomitant cardiovascular disease groups, BMI) | During observation period of three months |
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