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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00545636
Other study ID # SHEBA-07-4879-ZS-CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received October 16, 2007
Last updated June 7, 2012
Start date March 2008

Study information

Verified date June 2012
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date March 2009
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Children who are about to undergo anesthesia for elective medical interventions,

- Age 0-18 years

Study Design

Intervention Model: Single Group Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
education
The intervention is an education of the medical teams that instruct children to fast before the administration of general anesthesia

Locations

Country Name City State
Israel Sheba Medical Center Tel Hashomer

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Education of the medical teams as to preoperative fasting time will aid in shortening of an unnecessary prolonged fasting Immediate pre-anesthesia period (to assess lenth ofpreoperative fasting time) No