Adherence of PREprocedural eating and drinking before a oesophasal-gastro-duodenoSCOpy to shorten prolonged fasting: A pilot study
Completed
- Conditions
- fastinggastric investigationgastroscopy10018012
- Registration Number
- NL-OMON49346
- Lead Sponsor
- Ziekenhuisvoorzieningen Gelderse Vallei
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 48
Inclusion Criteria
patients who are planned for gastroduodenoscopy at outpatient clinic basis;
• if they were 18 years old and beyond,
• if they were able to consume foods per mouth
• provided informed consent.
Exclusion Criteria
• patients who have had bariatric surgery
• patients with had a clinical proven gastropareses or absence of swallow reflex
• patients with diabetes mellitus
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primary feasibility outcomes are reach and recruitment, dose received, fidelity<br /><br>and limited efficacy. Reach and recruitment will be measured with inclusion<br /><br>rate and barriers to participate. Dose will be measured as patients<br /><br>satisfaction and barriers for adherence. Fidelity will be measured with<br /><br>adequate fasting time. Limited efficacy will be estimated with gastric<br /><br>visibility and comfort. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary effectiveness outcomes are time of procedures, and complications. </p><br>