A Research Study Looking at How Semaglutide Works in People With Type 2 Diabetes in Switzerland, as Part of Local Clinical Practice (SURE SWITZERLAND)

Novo Nordisk A/S215 enrolled

Overview

The purpose of the study is to collect information on how semaglutide works in real world patients. Participants will get semaglutide prescribed by the study doctor. The study will last for about 6 to 8 months. Participants will be asked to complete some questionnaires about their health and diabetes treatment. Participants will complete these questionnaires during their normally scheduled visits with the study doctor.

Study Type

OBSERVATIONAL

Enrollment

215

Conditions

Diabetes Mellitus, Type 2

Interventions

SemaglutideDRUG

Patients will be treated with commercially available semaglutide in a prefilled pen injector (FlexTouch® variant) according to routine local clinical practice at the discretion of the treating physician. Other anti-hyperglycaemic treatments will be prescribed at the physician's discretion.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Signed informed consent obtained before any study-related activities (study-related activities are any procedures related to recording of data according to protocol) * The decision to initiate treatment with commercially available semaglutide has been made by the patient/Legally Acceptable Representative and the treating physician before and independently from the decision to include the patient in this study * Male or female, age greater than or equal to 18 years at the time of signing informed consent * Diagnosed with type 2 diabetes at least 12 weeks prior to inclusion * Available and documented haemoglobin A1c (HbA1c) value less than or equal to 12 weeks prior to initiation of semaglutide treatment Exclusion Criteria: * Previous participation in this study. Participation is defined as having given informed consent in this study * Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation * Treatment with any investigational drug within 90 days prior to enrolment into the study * Hypersensitivity to semaglutide or to any of the excipients

Locations (28)

Outcomes

Primary Outcomes

Change in Glycated Haemoglobin A1c (HbA1c)

Measured in % points

Time frame: Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)

Change in HbA1c

Measured in mmol/mol

Time frame: Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)

Secondary Outcomes

Change in body weight

Measured in kg

Time frame: Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)

Change in body weight

Measured in %

Time frame: Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)

Change in waist circumference

Measured in cm

Time frame: Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38)

HbA1c level at end of study: <8.0% (64 mmol/mol) (yes/no)

Number of participants who achieved/not achieved HbA1c level at end of study: \<8.0%

Time frame: At end of study (week 28 to 38)

HbA1c level at end of study: <7.5% (59 mmol/mol) (yes/no)

Number of participants who achieved/not achieved HbA1c level at end of study: \<7.5%

Time frame: At end of study (week 28 to 38)

HbA1c level at end of study: <7.0% (53 mmol/mol) (yes/no)

Data from ClinicalTrials.gov

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