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NCT05123768: GenCP

Genetic Etiology in Patients With Cerebral Palsy

Completed Last updated 2 November 2022
What this trial tests

trial testing NGS in Cerebral Palsy in 150 participants. Completed in 1 November 2022.

Timeline
1 April 2021
Primary endpoint
1 July 2022
1 November 2022

Quick facts

Lead sponsorUniversity Medical Centre Ljubljana
StatusCompleted
Study typeOBSERVATIONAL
Enrollment150
Start date1 April 2021
Primary completion1 July 2022
Estimated completion1 November 2022
Sites1 location across Slovenia

Drugs / interventions tested

Conditions studied

Sponsor

University Medical Centre Ljubljana

Who can join

Adults 5 to 25, any sex, with Cerebral Palsy or Genetic Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Cerebral palsy (CP) is a permanent disorder of movement or posture due to non-progressive impairments of the developing brain. Current estimates indicate that as many as 30% of CP cases may be genetic in nature. In our study, the investigators will re-examine the data of children with CP, who are registered in the Slovenian National Registry of Cerebral Palsy. All children will be invited to the University Children's Hospital, University Medical Centre Ljubljana, where they will be re-examined by a neurologist. Blood for genetic testing will be taken. In the case of confirmed genetic ethiology of CP, the search for specific therapy will be possible.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Unravelling genetic etiology of cerebral palsy: findings from a Slovenian pediatric cohort.
    Arkar Silan U, Trebše A, Kovač J, Rogac M, et al · · 2025 · cited 1× · PMID 40771987 · DOI 10.3389/fneur.2025.1615449

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Other trials of NGS

Trials testing the same drug.

Other recruiting trials for Cerebral Palsy

Currently open trials in the same condition.

Other University Medical Centre Ljubljana trials

Trials by the same sponsor.

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Data sources for this page

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