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Observance of Preoperative Fasting Time a Before-and-after Sensitization Campaign to Fasting Guidelines Study

NCT05743803 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 364

Last updated 2023-09-28

No results posted yet for this study

Summary

The goal of this before and after observational study is to evaluate the impact of a global sensitization campaign (targeted on surgeons, anesthetist and patients) about pre-operative fasting in an adult population. The main questions it aims to answer are:

* Does the sensitization campaign reduce fasting time?
* Does reduce fasting time increase quality of post-operative recovery?

Sensitization campaign will be performed between the before and after phases, it will include:

* Planned and repeated mandatory on site lecture about pre-operative guidelines for surgeons, anesthetists and paramedics.
* Reminder display in surgical wards and consults.
* Individualized fasting cards for patients.
* Short message service reminder on pre-operative fasting rules for patients.
* Medical fasting prescription with clear fasting times.

Conditions

  • Fasting

Interventions

OTHER

Sensititization campaign on preoperative fasting rules

* Planned and repeated mandatory on site lecture about pre-operative guidelines for surgeons, anesthetists and paramedics. * Reminder display in surgical wards and consults. * Individualized fasting cards for patients. * Short message service reminder on pre-operative fasting rules for patients. * Medical fasting prescription with clear fasting times.

Sponsors & Collaborators

  • University Hospital, Angers

    lead OTHER_GOV

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-27
Primary Completion
2023-07-20
Completion
2023-08-20

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05743803 on ClinicalTrials.gov