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Metformin Therapy in Type 1 Diabetes Mellitus.

Application of Metformin as Adjuvant Therapy in Overweight and Obese Patients With Type 1 Diabetes Mellitus.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01889706
Enrollment
200
Registered
2013-06-28
Start date
2009-01-31
Completion date
2014-02-28
Last updated
2013-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Loss of Control of Diabetes

Keywords

Type 1 diabetes mellitus,, metformin,, insulin resistance,, obesity

Brief summary

The use of exogenous insulin and incorrect nutritional habits are conducive to obesity and excess weight. This leads to the development of insulin resistance, even in patients with type 1 diabetes mellitus. The purpose of this study is to assess the effects of metformin as adjunctive therapy on anthropometric parameters, insulin resistance and metabolic control in overweight and obese patients with type 1 diabetes mellitus. The study group consists of 200 Caucasian type 1 diabetic patients with elevated adipose tissue content as measured by electrical bioimpedance, treated at the Poznan University of Medical Sciences Department of Diabetology in 2009-2014. All patients have type 1 diabetes diagnosed by autoimmune antibodies, and are treated with intensive insulin therapy. This group is divided into metformin treated arm (group I+ M, 100 subjects), the remaining 100 patients are treated with insulin alone (control group, group I). Metformin is administered at least 6 months at a mean dose of 1000 mg/day. The investigators would like to assess the impact of metformin treatment on metabolic control, insulin resistance and anthropometric parameters in overweight and obese patients with type 1 diabetes.

Interventions

None listed

Sponsors

Poznan University of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* age \> 18 years \<60 years, * duration of diabetes \>3 years, * lack of metabolic control- HbA1C\>7,5% (despite participation in 5-day WHO education program) * treated with intensive insulin therapy

Exclusion criteria

* metabolically decompensate diabetes with acetonuria, * suspected lack of compliance, * lack of glucose and ketones self-monitoring, * hypoglycaemic unawareness or recurrent severe hypoglycemia (defined as more than two episodes of hypoglycemia lowered than 60 mg/dl with loss of consciousness, required assistance to treat) in the past 3 months, * recurrent diabetic ketoacidosis (more than two episodes in the past year) * another serious medical illness, * pregnancy or sexually active woman unwilling to take birth control. * renal impairment (estimated on the value calculated glomerular filtration rate using the MDRD formula-estimated glomerular filtration rate, eGFR\<45 mL / min * liver cell damage Alanine aminotransferase (ALT), Aspartate aminotransferase (AST) greater than twice the upper normal limit), * history of drug or alcohol abuse or those who used this drug before * changes in the way of antihypertensive and antihyperlipemic treatment.

Design outcomes

Primary

MeasureTime frameDescription
Body fat content and anthropometric parameters6 monthsassessed by electrical bioimpedance using a Tanita BC-418 MA device,

Secondary

MeasureTime frameDescription
Assessment of metabolic control6 months(HbA1C, lipid profile)
Insulin requirement3 , 6 months

Other

MeasureTime frameDescription
Assessment of skin AGE6 monthsAGE-Reader ( Diagn-Optic)

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026