Clinical Trials Directory

Trials / Completed

CompletedNCT07231666

Optimised Osmolality in Oral Supplements Optimised Osmolality in Oral Supplements

Goldilocks' Zone: Optimised Osmolality in Supplements for the Patient With an Ileostomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
University of Aarhus · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

14 patients with ileostomies were included in a quasi-randomized, crossover intervention study. Each patient ingested between 3-18 different supplements during separate 6-hours intervention periods. Ileostomy output and urine volume will be collected. Outcome measures include faecal wet-weight, urine volume, electrolytes, osmolality, and body composition measured with bioelectrical impedance analysis.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTwateroral commercially available supplements
DIETARY_SUPPLEMENTsemi skimmed milk or poweradeoral commercially available supplements
DIETARY_SUPPLEMENTjuiceoral commercially available supplements

Timeline

Start date
2021-11-11
Primary completion
2022-07-30
Completion
2022-10-31
First posted
2025-11-17
Last updated
2025-11-17

Locations

2 sites across 1 country: Denmark

Source: ClinicalTrials.gov record NCT07231666. Inclusion in this directory is not an endorsement.