Diabetes Mellitus, Type 2
Conditions
Brief summary
The purpose of the study is to collect information on how semaglutide works in real world patients. Participants will get semaglutide prescribed by their study doctor. The study will last for about 6 to 8 months. The participants will be asked to complete some questionnaires about their health and their diabetes treatment. Participants will complete these during their normally scheduled visits with their study doctor.
Interventions
DRUGsemaglutide
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.
Sponsors
Novo Nordisk A/S
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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 18 years or older 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 equal to or below 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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Glycated Haemoglobin A1c (HbA1c) | Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38) | Percent point |
| Change in HbA1c | Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38) | mmol/mol |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in waist circumference | Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38) | cm |
| HbA1c level below 8.0% (64 mmol/mol) (yes/no) | At end of study (week 28 to 38) | Number of participants |
| HbA1c level below 7.5% (59 mmol/mol) (yes/no) | At end of study (week 28 to 38) | Number of participants |
| HbA1c level below 7.0% (53 mmol/mol) (yes/no) | At end of study (week 28 to 38) | Number of participants |
| Reduction in HbA1c of 1.0% point or more (yes/no) | Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38) | Number of participants who achieved/not achieved reduction in HbA1c of 1.0% point or more |
| Weight reduction of 3.0% or more (yes/no) | Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38) | Number of participants who achieved/not achieved weight reduction of 3.0% or more |
| Weight reduction of 5.0% or more (yes/no) | Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38) | Number of participants who achieved/not achieved weight reduction of 5.0% or more |
| Change in body weight (kg) | Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38) | kg |
| Patient reported severe or documented hypoglycaemia (yes/no) | Between baseline (week 0), end of study (week 28-38) | Count |
| Change in score for Diabetes Treatment Satisfaction Questionnaire - Status (DTSQs) (absolute treatment satisfaction): Total treatment satisfaction | Baseline (week 0), end of study (week 28 to 38) | The status version (DTSQs) provides a measure of how satisfied patients are with their current diabetes treatment. It consists of 8 questions, which are to be answered on a Likert scale from 0 to 6 (0 = very dissatisfied to 6 = very satisfied). Six questions are summed to produce a total Treatment Satisfaction score. The remaining two questions are concerning perceived frequency of hyperglycaemia and perceived frequency of hypoglycaemia, respectively |
| Change in score for Diabetes Treatment Satisfaction Questionnaire - Change (DTSQc) (relative treatment satisfaction): Total treatment satisfaction | Baseline (week 0), end of study (week 28 to 38) | The change version (DTSQc) has the same 8 items as the status version, but is reworded to direct the patients to compare the experience of the current treatment with the experience of previous treatment. Each question is scored on a scale of -3 to +3 (-3 = much less satisfied now to +3 = much more satisfied now), with 0 (midpoint), representing no change |
| Change in score for Short Form (SF)-36 v2: Physical summary component | Baseline (week 0), end of study (week 28 to 38) | The SF-36®v2 questionnaire has 36 questions grouped into eight domains termed: physical functioning, bodily pain, role-physical, general health, vitality, social functioning, role-emotional and mental health, which again can be combined to give two summary component scores (overall mental- and physical health). |
| Change in score for SF-36 v2: Mental summary component | Baseline (week 0), end of study (week 28 to 38) | The SF-36®v2 questionnaire has 36 questions grouped into eight domains termed: physical functioning, bodily pain, role-physical, general health, vitality, social functioning, role-emotional and mental health, which again can be combined to give two summary component scores (overall mental- and physical health). |
| Patient completed the study under treatment with semaglutide (yes/no) | At end of study (week 28 to 38) | Count |
| HbA1c reduction of 1.0% point or more and weight reduction of 3.0% or more (yes/no) | Baseline (up to 12 weeks prior to treatment initiation at week 0), end of study (week 28 to 38) | Number of participants who achieved/not achieved HbA1c reduction of 1.0% point or more and weight reduction of 3.0% or more |
| Change in body weight (%) | Baseline (up to 12 weeks prior to treatment initiation (week 0) to end of study (week 28 to 38) | Percent |
Countries
Germany
Outcome results
None listed