Gastric Content in Fasting Volunteers and in Tirzepatide Users: an Observational and Cross-sectional Study

OBJECTIVES

1. Primary objective The primary objective is to evaluate the prevalence of a full stomach through gastric ultrasonography in volunteers who are using tirzepatide and have been fasting for at least 8 hours for solids and 2 hours for clear liquids.
2. Secondary objectives The secondary objectives are to evaluate whether the volunteers' demographic characteristics, duration of medication use, time elapsed since the last dose of tirzepatide, dose and dosing regimen, reason for medication use, and the presence of symptoms such as nausea, vomiting, and a sensation of gastric fullness may influence gastric emptying when these individuals are evaluated by ultrasonography.
3. STUDY DESIGN 2.1 Study design Observational, cross-sectional, non-interventional study. Study flowchart Below we present a schematic illustration of the study design.
4. STUDY POPULATION 3.1 Center and population Thirty volunteers will be included in the study, of whom 15 must be currently using tirzepatide and 15 must not be using the medication.

Potential volunteers may be invited in person, such as coworkers, individuals from their social circle, or even patients already referred to the Center for Interventional Medicine for other examinations/procedures.

The approach may also be carried out via WhatsApp message through the following invitation:

"You are being invited to participate in a study entitled 'Ultrasonographic evaluation of gastric content in fasting volunteers using Tirzepatide: an observational and cross-sectional study.' If you are using tirzepatide, we would like to invite you to participate in this study, which investigates gastric content in individuals with 8 hours of fasting through an abdominal ultrasonography examination. If you are interested in participating, please contact Dr. Guilherme Araújo at the phone number (11) 95638-2319." The process of obtaining the Informed Consent Form (ICF) will be conducted by the principal investigator or by a duly trained and delegated member of the research team, in person, prior to performing the ultrasonography examination. Thus, the consent process-namely, after understanding the study and voluntary confirmation of participation-must be obtained through a signed physical ICF before participation. After signing, the participant will receive a fully signed copy. A note will be made in the patient's medical record indicating the date on which the ICF was applied.

After inclusion in the study, gastric ultrasonography will be performed at Hospital Israelita Albert Einstein by an anesthesiologist experienced in gastric ultrasound. Images will be recorded in the PACS system (Picture Archiving and Communication System) and reviewed by a radiologist.

1. INCLUSION CRITERIA Adult individuals (age ≥ 18 years). Individuals currently using the medication tirzepatide. Individuals who have fasted for at least 8 hours for solids and 2 hours for clear liquids without residues.

4.1. Exclusion criteria Pregnant and postpartum individuals. Individuals with technical limitations for gastric content assessment by ultrasound (see definitions, section 5.3.3).

Presence of risk factors for gastroparesis (see definitions, section 3.2). Use of prokinetic medications that accelerate gastric emptying, such as bromopride, metoclopramide, and domperidone.

5.4 Sample size calculation Based on the literature (16), individuals in the control group presented residual gastric fluid areas ranging from 3 cm² to 7 cm², with a median area of 5.1 cm², which respectively correspond to 32.4 mL, 90.8 mL, and 63.1 mL of residual gastric fluid volume after 8 hours of fasting. Assuming an average increase of at least 20 mL of fluid in patients using semaglutide, with 95% confidence and 80% power, the required sample size for the study is 14 patients per group. To compensate for potential losses, the sample size will be increased by 10%, resulting in 15 volunteers in each group. Solid residue assessment will be descriptive, as any amount classifies the individual as having a full stomach. Furthermore, it is expected that individuals without risk factors for gastroparesis will present no solid residue after the recommended fasting period (8), making sample size calculation not feasible.