The goal of this clinical trial is to assess differences in residual gastric volumes after stopping Miralax ingestion at different time points (1-4 hours) prior to anesthesia induction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
200
Stopping Miralax ingestion 4 hours prior to anesthesia induction
Stopping Miralax ingestion 3 hours prior to anesthesia induction
Stopping Miralax ingestion 2 hours prior to anesthesia induction
Residual gastric volume as measured by EGD
Time frame: To be performed at the start of the EGD immediately after anesthesia induction.
Preoperative gastric POCUS volume assessment
Time frame: Performed prior to anesthesia induction
Effectiveness of colonoscopy cleanout
The effectiveness of colonoscopy cleanout will be assessed by the Boston Bowel Preparation Scale (BBPS).
Time frame: Performed during the colonoscopy portion following upper GI endoscopy (EGD)
Incidence of aspiration on induction and perioperative aspiration
Time frame: On anesthesia induction
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Stopping Miralax ingestion 1 hour prior to anesthesia induction