WithdrawnNot Applicable

Clears On the Day of Anesthesia Permissible up to One-Hour Prior (CODA-POP) to Surgery

Stopped: PI passed away

United States0Started 2024-01-20

Plain-language 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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Undergoing laparoscopic cholecystectomy during the day or night of a weekday (including those consented on a Friday who get postponed to a weekend surgery start time). * Modified rapid sequence intubation (mRSI) Exclusion Criteria: * History of reflux disease * History of hiatal hernia * History of esophageal disease * History of gastroparesis * Known history of difficult airway or planned fiberoptic intubation * HbA1c greater than 12 * Pregnant women * Prisoner * Procedures conducted on weekends and holidays * Emergency or non-elective procedures

What they're measuring

Residual Gastric Volume in mL/kg

Timeframe: At time of intubation (about 1 hour after fluid intake)

Trial details

NCT IDNCT06216977

SponsorThe University of Texas Health Science Center, Houston

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-05-30

View on ClinicalTrials.gov More Perioperative Nutrition trials