MedTrace Logo

Optimised Osmolality in Oral Supplements Optimised Osmolality in Oral Supplements

NCT07231666 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14

Last updated 2025-11-17

No results posted yet for this study

Summary

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

Conditions

  • Ileostomy - Stoma
  • Intestinal Failure

Interventions

DIETARY_SUPPLEMENT

water

oral commercially available supplements

DIETARY_SUPPLEMENT

semi skimmed milk or powerade

oral commercially available supplements

DIETARY_SUPPLEMENT

juice

oral commercially available supplements

Sponsors & Collaborators

  • University of Aarhus

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-11
Primary Completion
2022-07-30
Completion
2022-10-31

Countries

  • Denmark

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07231666 on ClinicalTrials.gov