Study type

Study type

Non-interventional study
Non-interventional study

Non-interventional study design

Cohort
Study drug and medical condition

Name of medicine, other

GLP-1 receptor agonists

Medical condition to be studied

Suicidal ideation
Self-injurious ideation
Suicide attempt
Completed suicide

Additional medical condition(s)

Self-injury/self-harm
Population studied

Short description of the study population

The population eligible for the study will consist of patients:
- registered with a GP-practice covered by IQVIA™ Medical research data (IMRD),
- who initiated treatment with GLP-1 receptor agonists or SGLT-2 inhibitors (new users) during the study period,
- who had not used GLP-1 receptor agonists or SGLT-2 inhibitors before index-date (i.e., date of index treatment initiation and the start of follow-up in the study),
- with at least one year (365 days) of recorded medical history prior to index-date,
- with at least one diagnosis of T2DM before index-date,
- with no history of suicide-related or self-harm-related events prior to index-date,
- who have been treated with biguanides (e.g., metformin, which is considered first-line antidiabetic treatment according to NICE guidelines (NICE, 2022)) before index-date.

No exclusion will be applied according to age.

Age groups

All
Study design details

Main study objective

Is the use of GLP-1 receptor agonists associated with an increased risk of suicide-related and self-harm-related events when compared to patients who are prescribed SGLT-2 inhibitors among T2DM patients?
Documents
Study report
English (4.35 MB - PDF)View document