Incidence of Compliance to the ASA Preoperative Fasting Guidelines in Elective Surgery
1 other identifier
observational
309
1 country
1
Brief Summary
Patients scheduled for elective surgery with general anesthesia, regional anesthesia, or procedural sedation and analgesia will be interviewed about the last time having
- clear liquid drink
- light meal
- regular meal
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2020
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 25, 2020
CompletedFirst Posted
Study publicly available on registry
December 11, 2020
CompletedStudy Start
First participant enrolled
December 26, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2022
CompletedJanuary 10, 2023
January 1, 2023
1.3 years
November 25, 2020
January 9, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
compliance to NPO guideline
definition of compliance include complete order of NPO for regular diet for 8 hours and soft diet for 6 hours and clear liquid for 2 hours.
8 hour
Study Arms (1)
Patients scheduled for general surgery with anesthesia
Patients scheduled for general surgery with anesthesia, receiving Nil-per-Oral order.
Interventions
Eligibility Criteria
Patients scheduled for elective surgery requiring general anesthesia, regional anesthesia, or procedural sedation and analgesia
You may qualify if:
- Scheduled for elective surgery requiring general anesthesia, regional anesthesia, or procedural sedation and analgesia.
You may not qualify if:
- Patients with the order of NPO after midnight.
- Patients with pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Medicine Siriraj Hospital, Mahidol University
Bangkok, 10700, Thailand
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Sirilak Suksompong, MD
Mahidol University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
November 25, 2020
First Posted
December 11, 2020
Study Start
December 26, 2020
Primary Completion
May 1, 2022
Study Completion
May 1, 2022
Last Updated
January 10, 2023
Record last verified: 2023-01
Data Sharing
- IPD Sharing
- Will not share