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Study identifier: NCT07641361 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Hydration Intervention to Decrease Side Effects Associated With GLP - 1 RA Therapy

Condition: Obesity & Overweight · Type 2 Diabetes · Type 2 Diabetes (Adult Onset)  ·  Sponsor: State University of New York at Buffalo

PhaseNA
Planned participants30
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

This is a 17 - week study consisting of a one - week run - in period and a 16 - week intervention. The 16 - week pilot interventions aims to increase hydration in those beginning GLP - 1 RA therapy. Investigators aim to increase hydration to potentially decrease side effect severity, amount of side effects, and drug discontinuation associated with GLP - 1 RA therapy. The investigators are piloting to assess feasibility and preliminary efficacy of the intervention through examining participant retention, participant feedback, researcher and participant adherence to protocols, impact on hydration biomarkers, and participant reported GLP - 1 RA side effects.

This description comes directly from the study's public registry record.

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Locations (1)

State University of New York at Buffalo, South CampusBuffalo, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07641361