LivingGLP1
Study S000649

Prospective, Randomized, Controlled Trial of Preoperative Use of Saxenda (Liraglutide) Additionally to Common Dietological Measures as Opposed to Dietological Measures Alone

Registration

Registration
NCT06865365
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE4
Masking
NONE
Status
NOT_YET_RECRUITING
Enrollment
72
Start
2025-05-01
Primary completion
2027-02-01
Lead sponsor
Medical University of Vienna
Conditions
Obesity, Adolescent
Interventions
DRUG:Liraglutide daily (0.6-3.0mg, highest tolerable dose) additional to dietological measures and lifestyle optimization suggestions; BEHAVIORAL:Dietologic measures and lifestyle optimization for weight loss
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • % total weight loss [body weight and bmi will be assessed immediately when admission to the study is done as reference value and at at time of operation, which is 6 months after admission to the study, as outcome value]

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