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Quality Improvement Project to Reduce Preoperative Fasting Times Before Elective Procedures

Quality Improvement Project to Reduce Preoperative Fasting Times Before Elective Procedures

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07488468
Enrollment
1000
Registered
2026-03-23
Start date
2026-01-30
Completion date
2026-07-30
Last updated
2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium, Perioperative Patient Comfort / Quality of Care, Postoperative Nausea and Vomiting (PONV), Postoperative Pulmonary Complications, Preoperative Fasting

Keywords

Preoperative fasting, clear liquids, quality improvement

Brief summary

This single-center quality improvement project evaluates preoperative fasting times before elective procedures requiring anesthesiology care. The project aims to reduce prolonged fasting for clear fluids by implementing a local standard operating procedure (SOP) allowing patients to drink clear liquids until being called to the operating room ("drink until called"), supported by staff education and fasting instruction cards. Fasting times and selected perioperative outcomes will be assessed before and after implementation.

Detailed description

Traditionally, surgical patients are instructed to fast for prolonged periods to reduce the risk of pulmonary aspiration. International guidelines recommend fasting from clear liquids for 2 hours prior to elective procedures, yet real-world fasting often extends to 6-10 hours, which can impair patient well-being and may contribute to complications such as dehydration, hypoglycemia, postoperative nausea and vomiting, and delirium-particularly in older or frail patients. This quality improvement project follows the Plan-Do-Study-Act (PDSA) framework. Plan: Review evidence and decide to implement "drink until called to the OR." Do: Train anesthesiology staff, adapt local SOPs, provide oral patient instructions, and introduce fasting instruction cards for patients and staff. Study: Record and analyze fasting times and fluid intake prior to anesthesia induction; assess effectiveness and adjust strategies. Act: Add further staff education, posters, and short instructional screencasts to reinforce the updated fasting guidance.

Interventions

None listed

Sponsors

University of Giessen
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All patients elective surgery or intervention requiring with anesthesiology care general anesthesia, regional anesthesia, sedation, or anesthesiology stand-by

Exclusion criteria

* Already sedated, intubated, and mechanically ventilated patients

Design outcomes

Primary

MeasureTime frameDescription
Preoperative fasting time (clear liquids and solids)At anesthesia induction.Time interval between last intake of clear liquids and anesthesia induction. Time interval between last solid meal and anesthesia induction.
PACU length of stayPACU admission to discharge.PACU length of stay

Secondary

MeasureTime frameDescription
Preoperative fasting time (clear liquids and solids)At anesthesia induction (pre vs post implementation periods).Time interval between last intake of clear liquids and anesthesia induction. Time interval between last solid meal and anesthesia induction.
Patient satisfaction regarding fastingimmediately after the intervention/procedure/surgery up to 1 day postoperativelyPatient satisfaction regarding fasting (questionnaire)
Perioperative complicationsIntraoperative and immediate postoperative period (PACU).Perioperative complications (e.g., nausea, vomiting, regurgitation/aspiration)
Postoperative pulmonary and gastrointestinal complicationsDuring the hospital stay up to 30 daysPneumonia,Aspiration, nausea and vomiting
Delirium occurrenceDuring the hospital stay, up to 30 daysOccurance of postoperative delir
Hospital length of stay and in-hospital mortalityUntil hospital discharge / up to 30 daysHospital length of stay and in-hospital mortality
Acute kidney injury (AKI)Within the first 3 postoperative days.Acute kidney injury (AKI) (creatinine increase)
ICU/IMC admissionDuring the hospital stay up to 30 daysICU/IMC admission (planned/unplanned) and duration

Countries

Germany

Contacts

CONTACTMarit Habicher, Dr.
Marit.Habicher@chiru.med.uni-giessen.de+4964198544401
CONTACTBrigitte Clausen
Brigitte.Clausen@chiru.med.uni-giessen.de

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026