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Clinical Trial Summary

The purpose of this study is to assess whether residual gastric volumes in patients who receive clear liquids one hour prior to time of procedure is non-inferior compared to patients who are NPO past midnight, to compare efficiency and flexibility of operating room scheduling between two fasting conditions, to assess patient satisfaction and post-operative nausea, vomiting, pain, hunger and thirst. and to assess wound healing and post-operative complication rates.


Clinical Trial Description

n/a


Study Design


NCT number NCT06216977
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact George Williams, MD, FASA, FCCM, FCCP
Phone (713) 500-6680
Email George.W.Williams@uth.tmc.edu
Status Not yet recruiting
Phase N/A
Start date January 20, 2024
Completion date July 1, 2024