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NCT07616908
Effect of Miralax NPO Time on Residual Gastric Volumes and Bowel Preparation
Conditions: Residual Gastric Contents, Polyethylene Glycol
Sex: All
Ages: N/A – 18 Years
Healthy volunteers: No
Phase: NA
Enrollment: 200
Sponsor: Stanford University
Summary
The goal of this clinical trial is to assess differences in residual gastric volumes after stopping Miralax ingestion at different time points (2, 4, 6 hours) prior to anesthesia induction and compare it to the control (current institutional standard of care where no Miralax is given on the day of surgery).
Eligibility Criteria
Inclusion Criteria:
* Patients undergoing both EGD and colonoscopy
* Use of Miralax for cleanout
* Patients \
Source: ClinicalTrials.gov (NCT07616908). StuddyBuddy aggregates publicly available trial information.
