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Clinical Trial Summary

Our objective is to compare gastric volumes (mL) between women who receive metoclopramide versus placebo prior to scheduled cesarean delivery in appropriately fasted patients. If metoclopramide is found not to reduce gastric volumes this would inform future practice guidelines for obstetric anesthesia, which currently recommends metoclopramide administration prior to cesarean deliveries. We hypothesize that metoclopramide given to women with appropriate fasting prior to cesarean delivery does not result in any clinically significant reduction in gastric volume (mL) and therefore does not provide any additional benefit for aspiration prophylaxis but may expose patients to unnecessary side effects. A secondary objective will be to evaluate if gastric volume is a significant predictor of intraoperative nausea and vomiting.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05033041
Study type Interventional
Source Northwestern University
Contact Jennifer Banayan, MD
Phone (312) 472-3585
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date October 2021
Completion date April 2024

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