LivingGLP1
Study S001718

Comparison of Efficacy and Safety of POSE 2.0 Procedure Compared to GLP-1 Agonist in a Cohort of Patients for Management of Obesity: a Single-center Randomized Crossover-controlled Trial

Registration

Registration
NCT05705388
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Status
UNKNOWN
Enrollment
50
Start
2023-01-16
Primary completion
2025-01-03
Lead sponsor
Emirates Health Services (EHS)
Conditions
Obesity
Interventions
DEVICE:POSE2.0 Endoscopic Gastric Remodeling; DRUG:Liraglutide injection
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Mean percent total body weight loss at 6 months in each arm of the study [6 months]
  • Percentage of subjects with ≥5 percent total body weight loss at 6 months in each arm at 6 months [6 months]
  • The incidence, frequency, and severity of adverse events related to treatment with the device and procedure as well as medication will be reported. [at 6 months]

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