LivingGLP1
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

Registration
NCT07847593
Acronym
ProSem
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
102
Start
2025-07-09
Primary completion
2026-07-15
Lead sponsor
Nordic Biotic Sp. z o.o.
Conditions
Obesity (Disorder); GLP-1 Receptor Agonist Treatment; Probiotic Intervention; Diabetes Mellitus Type 2
Interventions
DIETARY_SUPPLEMENT:Four-strain probiotic formulation; DIETARY_SUPPLEMENT:Maltodextrin (Placebo)
Results posted
FALSE
Individual participant data sharing
NO

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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