Recruiting NCT06525753

Weaning is Winning? (WeWin Study)

— Observational Intestinal Failure Parenteral Nutrition

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Weaning off Parenteral Nutrition.
Who it may be relevant to: Registry conditions: Intestinal Failure, Parenteral Nutrition. Basic parameters: 0 years — 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Canada
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

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Official title

Weaning is Winning? (WeWin Study): Are Parenteral Nutrition (PN) Graduates Growing up Healthy?

Overview

We propose a multicenter prospective study on pediatric patients with intestinal failure (IF) who weaned off parenteral nutrition (PN).

Detailed description

Children with IF depend on PN. This is associated with frequent and various complications such as metabolic bone disease, micronutrient deficiencies and abnormal body composition. Due to advancements in care, many patients with IF are able to wean off PN; they are so called PN graduates. It is currently not well known how often complications do occur after weaning off PN, and which patients are at highest risk of developing these complications.

Interventions

Other Weaning off Parenteral Nutrition
pediatric intestinal failure patients who have been weaned off parenteral nutrition

Primary outcome measures

Complications [Time frame: From 1 year after weaning off PN to 18 years of age]

Eligibility criteria

Inclusion criteria

Parenteral Nutrition graduates for at least 1 year, with a history of intestinal failure.
Age <18 years at time of inclusion.

Exclusion criteria

No consent provided.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Case-only

Study locations

Canada · 1 center

The Hospital for Sick Children — Toronto

Identifiers

NCT: NCT06525753 · 1000080824

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗