Primary objective : To evaluate the efficacy (in terms of change in HbA1c readings starting from baseline then after 13 weeks \& at the end of the study which will be after 26 weeks) in subjects with type I diabetes mellitus. Secondary objective : * Recording the average daily dose of both insulin Glulisine \& insulin Glargine in type I DM. * Recording adverse events.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
98
in combination with insulin Glulisine as bolus regimen
in combination with insulin Glargine as bolus regimen
Sanofi-aventis administrative office
Manama, Bahrain
Sanofi-aventis administrative office
Kuwait City, Kuwait
Sanofi-Aventis Administrative Office
Doha, Qatar
Sanofi-aventis administrative office
Dubai, United Arab Emirates
Evaluating the Glycemic control of the regimen : Change in A1C levels
Time frame: from baseline to study end
Average daily dose : - For both insulin Glulisine & insulin Glargine. - FBG and PPBG if possible ?
Time frame: from baseline to study end
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