LivingGLP1
Study S002200

DUTCH Weight Control in Atrial Fibrillation Study, a Multi-center, Double-blind, Randomized, Parallel Group, Placebo-controlled Trial

Registration

Registration
NCT06184633
Acronym
DUTCH-WAIST
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
TRIPLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
280
Start
2024-07-21
Primary completion
2027-04-10
Lead sponsor
Rijnstate Hospital
Conditions
Atrial Fibrillation; Obesity; Weight Loss
Interventions
DRUG:Semaglutide 3.2 MG/ML; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • The primary efficacy clinical endpoint of the trial is assessed at 12 months by a 7 point scale. Only the worst clinical outcome will be retained as the primary efficacy outcome [At 1 year follow-up]

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