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Taking people in Dánia4. fázis

A Pragmatic Trial Comparing Empagliflozin and Dapagliflozin Through Cluster Randomization Embedded in the Electronic Health Record

Key facts

Where
Copenhagen, Herlev, Hillerød, Holbæk, Hvidovre, Køge, Nykøbing Falster, Rønne, Roskilde és Slagelse, DániaSee the 12 sites
Phase
4. fázis

Where in Dánia

  • Bispebjerg HospitalCopenhagen, DániaTaking people
  • RigshospitaletCopenhagen, DániaTaking people
  • Herlev and Gentofte HospitalHerlev, DániaTaking people
  • Steno Diabetes Center CopenhagenHerlev, DániaTaking people
  • Nordsjællands HospitalHillerød, DániaTaking people
  • Holbæk SygehusHolbæk, DániaTaking people
  • Hvidovre HospitalHvidovre, DániaTaking people
  • Sjællands UniversitetshospitalKøge, DániaTaking people
  • Nykøbing F. SygehusNykøbing Falster, DániaTaking people
  • Bornholms HospitalRønne, DániaTaking people
  • Sjællands UniversitetshospitalRoskilde, DániaTaking people
  • Slagelse SygehusSlagelse, DániaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Herlev and Gentofte Hospital
Trial code
NCT06642272
Record updated
2026. szeptember 18.
Original description
The aim of this clinical trial is investigate the comparative effectiveness of empagliflozin and dapagliflozin for the treatment of diabetes, chronic kidney disease, and heart failure.Read full original descriptionShow less

The aim of this clinical trial is investigate the comparative effectiveness of empagliflozin and dapagliflozin for the treatment of diabetes, chronic kidney disease, and heart failure.

Patients who are prescribed either empagliflozin or dapagliflozin, as part of daily clinical practice at the participating sites, will be included in the study. Treatment will be randomized automatically through the electronic health record software in clusters defined by time of day.

https://www.appletreestudy.com

Inclusion: Adults aged 18 years or more.

Exclusion: Incapabability of giving informed consent; Withdrawal of informed consent.

ClinicalTrials.gov NCT06642272