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NCT04273490

Characterising Pain, QoL, Body Composition, Arterial Stiffness, Muscles and Bones in Adult Persons With XLH and Healthy Controls

Completed Last updated 29 November 2023
What this trial tests

trial in X-linked Hypophosphatemia in 92 participants. Completed in 20 December 2022.

Timeline
18 February 2020
Primary endpoint
20 December 2022
20 December 2022

Quick facts

Lead sponsorUniversity of Aarhus
StatusCompleted
Study typeOBSERVATIONAL
Enrollment92
Start date18 February 2020
Primary completion20 December 2022
Estimated completion20 December 2022
Sites1 location across Denmark

Conditions studied

Sponsor

University of Aarhus

Who can join

18 and older, any sex, with X-linked Hypophosphatemia or Hereditary Hypophosphatemia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hereditary hypophosphatemia (XLH) is a rare, inherited disease. Loss-of-function mutation in the phosphate regulating gene with homologies to endopeptidases on the X-chromosome (PHEX) results in excess fibroblast growth factor 23 (FGF23) production and manifests as rickets in children and osteomalacia in adults. This study aims to characterize and measure pain, quality of life, muscle function, body composition, arterial stiffness, bone mineral density, geometry and microarchitecture in patients with XLH compared to age and gender-matched controls.

Publications & conference data

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

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Other recruiting trials for X-linked Hypophosphatemia

Currently open trials in the same condition.

Other University of Aarhus 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/NCT04273490.

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