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Osmolality of Oral Supplements and Ileostomy Output

NCT03348709 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2018-11-05

No results posted yet for this study

Summary

This double-blinded, active comparator, cross-over intervention study tested the impact of two different oral supplements on ileostomy output volume and urinary sodium excretion and intestinal aquaporin expression in eight compensated patients with an ileostomy and not on home parenteral Nutrition or fluid support.

Conditions

  • Ileostomy - Stoma
  • Short Bowel Syndrome
  • Sodium Depletion
  • Nutritional Deficiency

Interventions

DIETARY_SUPPLEMENT

Isoosmolar

48 hours, 800 ml per 24 hours

DIETARY_SUPPLEMENT

Hyperosmolar

48 hours, 800 ml per 24 hours

Sponsors & Collaborators

  • University of Copenhagen

    collaborator OTHER

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Hendrik Vilstrup, Professor · University of Aarhus

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-01
Primary Completion
2018-06-01
Completion
2018-11-01

Countries

  • Denmark

Study Locations

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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 NCT03348709 on ClinicalTrials.gov