Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Type2 Diabetes
Type
Interventional
Phase
Phase 4
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

In this randomized, double-blind, parallel, placebo-controlled trial we compare the effects of semaglutide 1.34 mg/ml vs. normal dieting by randomizing the patients with both T2DM and overweight/obesity (BMI ?27) (n=50, aged ?18 to < 65 years) to two groups: both groups participate in a similar life...

In this randomized, double-blind, parallel, placebo-controlled trial we compare the effects of semaglutide 1.34 mg/ml vs. normal dieting by randomizing the patients with both T2DM and overweight/obesity (BMI ?27) (n=50, aged ?18 to < 65 years) to two groups: both groups participate in a similar lifestyle treatment to induce weight loss, but one group gets an add-on of semaglutide 1.34mg/ml while the other is treated with placebo. Additionally, a reference group of healthy normal weight non-diabetic individuals (BMI ? 25 kg/m2, n=25, aged ?18 to < 65 years) are included as controls at the initiation of the study.

Tracking Information

NCT #
NCT04854083
Collaborators
  • University of Helsinki
  • Turku University Hospital
Investigators
Principal Investigator: Kirsi Pietiläinen, MD PhD Helsinki University Central Hospital