CompletedNot Applicable

Optimised Osmolality in Oral Supplements Optimised Osmolality in Oral Supplements

Denmark14 participantsStarted 2021-11-11

Plain-language summary

Quasi-randomized, crossover intervention study, testing osmolality in oral drinks and effect on 6-hours ileostomy output in adult patients with an ileostomy

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. age 18 years or higher
✓. ileostomy formed at least 8 weeks before enrolment
✓. consent to participate

Exclusion criteria

✕. pregnancy
✕. known chronic kidney disease
✕. known diabetes mellitus
✕. too long driving distance
✕. parenteral nutrition/fluid more than 6 litres per month

What they're measuring

ileostomy output

Timeframe: 6 hours

Trial details

NCT IDNCT07231666

SponsorUniversity of Aarhus

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-07-30

View on ClinicalTrials.gov More Ileostomy - Stoma trials