LivingGLP1
Study S001993

Adjuvant Nutritional Therapy to Incretin-based Anti-obesity Medications in the Management of Gastrointestinal Adverse Events During the Up-titration Phase

Registration

Registration
NCT06431308
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
NONE
Status
RECRUITING
Enrollment
120
Start
2025-01-30
Primary completion
2026-02-01
Lead sponsor
Ariel University
Conditions
Obesity; Drug
Interventions
BEHAVIORAL:nutritional intervention
Results posted
FALSE

Registered primary outcomes

  • Gastrointestinal symptoms assessment [Baseline and at the end of the study period (20 weeks)]
  • Defecation texture [Baseline and at the end of the study period (20 weeks)]
  • Bowel Movement (BM) frequency [Baseline and at the end of the study period (20 weeks)]
  • Participants gastrointestinal symptoms report [Baseline, at the end of the study period (20 weeks) and weekly until 20 weeks (for subjective GI symptoms report only)]

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