The Influence of Education of Medical Team on Duration of Fasting Before Elective Medical Interventions Performed Under General Anesthesia in Children
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Purpose
The purpose of the study is to examine if an education program of the medical teams can help implementation of of NPO (nothing-per-os)orders in children before anesthesia for ambulatory medical interventions under anesthesia and decrease unnecessary long fasting. We shall ask parents of such children to fill in a questionnaire regarding pre-anesthesia fasting and regular eating and drinking habits. Thereafter, all medical teams involved with the administration of NPO orders will receive an educational program to explain and implement the NPO orders as are recommended by the American Society of Anesthesiologists. We will examine if the educational program was successful in reducing unnecessary long period of fasting, and if such a program is not associated with increased rate of delay of cases.
| Condition | Intervention |
|---|---|
|
Duration of Preoperative Fasting |
Other: education |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Single Blind (Caregiver) Primary Purpose: Prevention |
| Official Title: | The Influence of Education of Medical Team on Duration of Fasting Before Elective Medical Interventions Performed Under General Anesthesia in Children |
- Education of the medical teams as to preoperative fasting time will aid in shortening of an unnecessary prolonged fasting [ Time Frame: Immediate pre-anesthesia period (to assess lenth ofpreoperative fasting time) ] [ Designated as safety issue: No ]
| Enrollment: | 0 |
| Study Start Date: | March 2008 |
| Estimated Primary Completion Date: | March 2009 (Final data collection date for primary outcome measure) |
-
Other: education
Eligibility| Ages Eligible for Study: | up to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Children who are about to undergo anesthesia for elective medical interventions,
- Age 0-18 years
Contacts and Locations| Israel | |
| Sheba Medical Center | |
| Tel Hashomer, Israel, 52621 | |
| Principal Investigator: | Ze'ev Shenkman, MD | Sheba Medical Center, Department of Anesthsia C and Department of Anesthesia |
| Study Director: | Haim Berkenstadt, MD | Sheba Medical Center |
More Information
No publications provided
| Responsible Party: | Ze'ev Shenkman, MD, Sheba Medical Center |
| ClinicalTrials.gov Identifier: | NCT00545636 History of Changes |
| Other Study ID Numbers: | SHEBA-07-4879-ZS-CTIL |
| Study First Received: | October 16, 2007 |
| Last Updated: | June 7, 2012 |
| Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
Additional relevant MeSH terms:
|
Anesthetics Central Nervous System Depressants Physiological Effects of Drugs |
Pharmacologic Actions Central Nervous System Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on June 18, 2013