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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01133691
Other study ID # KEK-ZH-Nr. 2009-0147
Secondary ID
Status Completed
Phase N/A
First received May 11, 2010
Last updated January 16, 2012
Start date May 2010
Est. completion date February 2011

Study information

Verified date January 2012
Source University Children's Hospital, Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Swissmedic
Study type Observational

Clinical Trial Summary

- Background: Fasting is mandatory for safety of anesthesia in elective surgery and imaging but gives rise to discomfort, hunger and thirst especially in children. Internationally accepted fasting times are often prolonged because of organisational delay in operating theatre.

- Hypothesis: Clear fluids can be ingested until an imaginary anesthesia induction time without enlarging the residual gastric contents compared to overnight fast. There is no difference between residual gastric contents after 4 hours of fasting after a light meal compare to 6 hours in healthy children.

- Examination of gastric volume using magnetic resonance imaging after overnight fasting and subsequent scans after either clear fluid intake or intake of a standard breakfast are performed in children aged 6 - 12 years. Time course after fluid intake is followed with scans every half hour for 2 hours. In the breakfast group 4 versus 6 hours fasting time will be simulated, e. g. intake of clear fluid is allowed for 2 versus 4 hours after the meal. Volume of gastric contents will be compared with a standardized ultrasonographic view of the stomach.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date February 2011
Est. primary completion date February 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 6 Years to 12 Years
Eligibility Inclusion Criteria:

- age 6 - 12 years

- ASA I or II

Exclusion Criteria:

- gastrointestinal pathology

- claustrophobia

- implants like pacemaker, ventriculoperitoneal shunt etc

- symptomatic or relevant cardiac, renal or metabolic disease

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
clear fluid, light breakfast
clear fluid 7 ml/kg, breakfast consisting of yoghurt, muesli, mild

Locations

Country Name City State
Switzerland University Children's Hospital, Anesthesiology Zurich

Sponsors (1)

Lead Sponsor Collaborator
University Children's Hospital, Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gastric emptying time Time after food/fluid ingestion when gastric volume after overnight fast is achieved, as measured by volumetry of magnetic resonance scans 6 hours No
Secondary gastric volume after fasting 6 hours No
Secondary gastric antral area 6 hours No
Secondary visual analog scale of thirst/hunger 6 hours No
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