Study S000102
The Effect of Probiotics on Glucagon-Like Peptide-1 (GLP-1) Receptor Agonist Therapy in Patients With Obesity: A Randomized, Double-Blind, Controlled Trial
Registration
Registered primary outcomes
- Gastrointestinal adverse event incidence proportion during semaglutide treatment [During the 12-week semaglutide treatment and dose-escalation period]
- Prevalence of gastrointestinal adverse events during semaglutide treatment [During the 12-week semaglutide treatment and dose-escalation period]
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