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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06007521
Other study ID # 69HCL23_0804
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 18, 2023
Est. completion date December 18, 2024

Study information

Verified date January 2024
Source Hospices Civils de Lyon
Contact Eleni PANAGIOTAKAKI, Dr
Phone 04.27.85.60.60
Email eleni.panagiotakaki@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Alternating Hemiplegia of Childhood (AHC) is a very rare neurological disorder of genetic origin, combining paroxysmal episodes and neurodevelopmental impairment. The disease is generally sporadic, and its incidence has been estimated at 1 in 100,000 births, with around 500 cases published worldwide. The true prevalence of AHC may be underestimated due to a lack of understanding of the disease and a high degree of phenotypic heterogeneity. It should be noted that, to date, it is difficult to assess the clinical characteristics of AHC patients in a homogeneous way. The lack of disease-specific clinical outcome measures therefore constitutes a critical node for advancing AHC research. In addition, recognition of the pattern of movement disorders and the ability to classify their severity are very important and useful for the clinician. Homogeneous disease assessment will help plan rehabilitative and pharmacological interventions, facilitate monitoring of treatment outcomes, and predict prognosis. This is why an AHC assessment scale have been developed in collaboration with clinical teams from the IAHCRC consortium. The scale has already been tested and validated on Italian and Spanish patients. The aim of this study is therefore to validate the use of this same scale on our French population of AHC patients. The hypothesis of the study is that the practical use of this scale specific to alternating hemiplegia is reproducible. To this end, all the items on the scale will be scored independently for each patient by 4 neuropediatricians with expertise in the disease, in order to observe the reproducibility of the results obtained with this scale. The scale will be used for twenty AHC patients of all ages.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 18, 2024
Est. primary completion date December 18, 2024
Accepts healthy volunteers
Gender All
Age group 0 Years to 99 Years
Eligibility Inclusion Criteria: - Patient with confirmed diagnosis of AHC, unrestricted age range 0-99 years - At least one parent and/or legal guardian who understands and speaks the national language Adult patients : - Gathering of the non-opposition of the patient and/or his legal representative Minor patients : - Collection of non-opposition from parents/guardians Exclusion Criteria: - Patient's refusal to participate in the study - Patient under court protection, unable to give consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
interview with neurologist
interview with neurologist

Locations

Country Name City State
France Service d'Epileptologie Clinique, des Troubles du Sommeil et de Neurologie Fonctionnelle de l'Enfant Bron Rhone

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite primary endpoint : - missing data from the scale <5 - mean scores compared between the 4 neurologists are close to the scale's mid-point, i.e. floor and ceiling effects are < 20%, and skewness statistics are between 21 and 11 All statistical tests will be performed using SPSS version 24.0 statistical software, and P < 0.05 will be considered significant.
Validation of the use of the scale based on the results obtained independently by the 4 expert neurologists using a composite primary endpoint consisting of three criteria:
missing data from the scale <5
mean scores compared between the 4 neurologists are close to the scale's mid-point, i.e. floor and ceiling effects are < 20%, and skewness statistics are between 21 and 11.
At inclusion
See also
  Status Clinical Trial Phase
Completed NCT04020848 - Observe Alternating Hemiplegia of Childhood (OBSERV-AHC) Study