Evaluation of Gastric Content of Volunteers Fasting and Using Semaglutide: an Observational and Cross-sectional Study
- Sponsor
- Hospital Israelita Albert Einstein
- Study ID
- NCT06154486
- Status
- Completed
Conditions
- Anesthesia
- Pneumonia, Aspiration
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- semaglutide use — DRUGpatient using semaglutide for at least 7 days
Study Details
Medicines with peptide-1 receptor agonist action similar to glucagon (GLP-1) are a modern therapeutic option for obesity and diabetes mellitus. Semaglutide is a representative of this class medication whose mechanism of action can result in the slowing of gastric emptying and reduced gastric motility, a scenario that can increase the risk of pulmonary aspiration in individuals undergoing anesthesia and despite adequate fasting. Given the severity of the occurrence of bronchoaspiration, the action biological analysis of GLP-1 analogues on gastric function and incremental use of these medications, through gastric ultrasound, we will aim to evaluate the gastric contents of volunteers who do not have risk factors for bronchoaspiration, who will not undergo anesthesia, but are with the fasting recommended for this purpose and are using semaglutide, an analogue of GLP-1. Our hypothesis is that the majority of individuals using these medications have a full stomach even during fasting times recommended in the literature. In view of this, for this population we must adapt safety criteria during the anesthetic procedure.
Key Dates
- Start date
- Jun 19, 2023
- Status verified
- Sep 2023
- Primary completion
- Jun 19, 2023
- Completion
- Aug 22, 2023
Study Design
- Enrollment
- 30 participants (actual)
Arms
- Arm: semaglutide grouppatients without risk factors for gastroparesis, fasting for at least 8 hours, BMI less than 30 and currently using semaglutide
- Arm: control grouppatients without risk factors for gastroparesis, fasting for at least 8 hours, BMI less than 30 and who have never used semaglutide or another GLP-1 analogue
Primary Outcome Measure
prevalence of full stomach after fasting for at least 8 hours [ Time Frame: 1 day ]
Related Studies
- The Pediatric Anesthesia Quality Improvement ProjectRecruiting · The Society for Pediatric Anesthesia · Phoenix, Arizona
- Anesthetics and Analgesics in ChildrenRecruiting · Chi Dang Hornik · Stanford, California
- Lung Recruitment Maneuver as a Potential Predictor of Fluid Responsiveness in Mechanically Ventilated Pediatric PatientsRecruiting · Boston Children's Hospital · Boston, Massachusetts
- Enhanced Recovery After Surgery (ERAS) Total Knee Replacement (TKR) With a Transitional Pain ServiceRecruiting · Hospital for Special Surgery, New York · New York, New York