Overview

Efficacy and Safety of Oral Acarbose Treatment in Patients With Type 2 Diabetes Mellitus

Status:
Completed
Trial end date:
2013-05-01
Target enrollment:
0
Participant gender:
All
Summary
The Purpose of This Study is to Evaluate the Efficacy and Safety of Acarbose in Type 2 Diabetic Patients Using Two Different Formulations of Acarbose 50mg.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
EMS
Treatments:
Acarbose
Criteria
Inclusion Criteria:

- Patients must be able to understand the study procedures agree to participate and give
written consent.

- Diagnosed with type 2 diabetes mellitus (t2dm)b

- Female patients of childbearing potential (i.e., ovulating, pre-menopausal, not
surgically sterile) which agree to use a medically accepted contraceptive regimen for
the duration of the study.

Exclusion Criteria:

- Pregnancy or risk of pregnancy.

- Lactation

- Any pathology or past medical condition that can interfere with this protocol

- Other conditions deemed reasonable by the medical investigator as to the
disqualification of the individual from study participation.

- Known hypersensitivity / intolerance to acarbose or any of its excipients