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The Semaglutide Study

Fasting

The primary goal of this study is to evaluate the incidence of "full stomach" in fasting elective surgical patients on Semaglutide medication. The other goals are to study the impact of the time interval since the last dose of the medication on the incidence of full stomach and to develop evidence-based recommendations for the perioperative management of these patients.

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Conditions de participation

  • Sexe:

    ALL

  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

1. Patients scheduled for elective surgery at Toronto Western Hospital
2. Aged ≥ 18 years of age
3. American Society of Anaesthesia physical status classification I to III
4. Patients being treated with Semaglutide for at least 1 month

Exclusion Criteria:

1. Current pregnancy evidenced by positive urinary pregnancy test
2. Previous surgery of the upper gastrointestinal tract

Lieu de l'étude

Toronto Western Hospital
Toronto Western Hospital
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Jayanta Chowdhury

[email protected]
416-603-5800
Étude parrainée par
University Health Network, Toronto
Participants recherchés
Plus d'informations
ID de l'étude: NCT06420739