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NCT05909228

Bone Markers in Pediatric IF

Completed Last updated 16 January 2024
What this trial tests

trial in Intestinal Failure in 35 participants. Completed in 30 September 2023.

Timeline
31 March 2023
Primary endpoint
30 September 2023
30 September 2023

Quick facts

Lead sponsorThe Hospital for Sick Children
StatusCompleted
Study typeOBSERVATIONAL
Enrollment35
Start date31 March 2023
Primary completion30 September 2023
Estimated completion30 September 2023
Sites1 location across Canada

Conditions studied

Sponsor

The Hospital for Sick Children

Who can join

Adults 6 Weeks to 18, any sex, with Intestinal Failure or Osteoporosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Poor bone health is a well-recognized but poorly understood complication in children with intestinal failure (IF) who are dependent on parenteral nutrition (PN). Previously, we showed that children with IF have decreased bone turnover markers. It is currently unknown if optimization of parenteral nutrition is related to improved bone turnover markers. Serum concentrations of bone markers (osteocalcin, bone-specific alkaline phosphatase and c-telopeptide) will be measured in 30 IF patients treated at a multidisciplinary intestinal rehabilitation and home PN program at the Hospital for Sick Children and compared to bone markers in 30 age- and sex-matched healthy controls.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Intestinal Failure

Currently open trials in the same condition.

Other The Hospital for Sick Children trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05909228.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing