Evaluation of gastric volumen changes in dependence of the prefasting time

Not Applicable

• Conditions: gastric problems; K50; Crohn disease [regional enteritis]

• Registration Number: DRKS00005020
• Lead Sponsor: Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-05-19
• Study Completion: 2016-06-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Age 2-18 years
- Routine planned gastroscopy

Exclusion Criteria

- Diabetes
- Acute or chronic upper gastrointestinal obstruction
- Conditions with increased abdominal pressure (e.g. ascites)
- Gastric acid blocker therapy
- Cortison therapy
- Patients who need a rapid sequence induction

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
With this study we do hope to further demonstrate the safety of preoperative consumption of clear fluids up to two hours preoperatively. For this purpose we will collect the gastric fluid during gastroscopy for measuring the volume and pH.

Secondary Outcome Measures

Name	Time	Method
A second aim is to analyze a possible difference in the incidence of postoperative nausea and vomiting (PONV) between the two groups in correlation to the different fasting periods.