Study S001993
Adjuvant Nutritional Therapy to Incretin-based Anti-obesity Medications in the Management of Gastrointestinal Adverse Events During the Up-titration Phase
Registration
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)]
Linked records (0)
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