LivingGLP1
Study S000683

A Multi-centre, Prospective, Noninterventional Study Investigating the Effectiveness of Onceweekly Subcutaneous Semaglutide in a Real World Adult Population With Type 2 Diabetes

Registration

Registration
NCT03929679
Acronym
SURE NL
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
218
Start
2019-05-28
Primary completion
2020-11-24
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:U1111-1222-5565

Registered primary outcomes

  • 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)]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0008386Once-Weekly Semaglutide Use in Type 2 Diabetes: Real-World Data from the SURE Netherlands Observational Study.
Wolffenbuttel BHR, Advances in therapy
2023Nonrandomized studyPMID 36542260DOIcites ClinicalTrials.gov:NCT03929679; registry reference RESULT:36542260