LivingGLP1
Study S000346

A Multicentre, Prospective, Non-Interventional, Single-Arm Study Investigating Glycaemic Control and Patient-Reported Outcomes in Type 2 Diabetes Patients, Uncontrolled on DPP4i Treatment and Who Switch to Oral Semaglutide in a Real-World Setting in Italy

Registration

Registration
NCT05755360
Acronym
DOORS
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
291
Start
2023-02-21
Primary completion
2024-10-21
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1274-4674

Registered primary outcomes

  • Absolute change in glycated haemoglobin (HbA1c) (percentage [%]-point) [From informed consent and treatment initiation (week 0) to end of study (week 40 ± 4 weeks)]
  • Absolute change in glycated haemoglobin (HbA1c) (millimoles per mole [mmol/mol]) [From informed consent and treatment initiation (week 0) to end of study (week 40 ± 4 weeks)]

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