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Recruiting NCT06178120

Disease Progression in Women With X-linked Adrenoleukodystrophy

Observational X-linked Adrenoleukodystrophy

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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: X-linked Adrenoleukodystrophy. Basic parameters: from 18 years · Female.
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
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

An Observational Study to Assess Disease Progression in Women With X-linked Adrenoleukodystrophy

Overview

Observational, single-site prospective and minimally interventional study in women with X-linked adrenoleukodystrophy (ALD), conducted in France.

Detailed description

Patients accepting participation (after signing ICF) will be followed up to at least 2 years or until they started treatment for X-linked adrenoleukodystrophy (ALD) or withdraw consent, whichever occurs first. Follow-up will be extended beyond 2 years if deemed appropriate after an interim report. Tests and questionnaires will be assessed at baseline and yearly. If the study is extended, beyond 2 years, patients will be assessed at 1-year intervals.

At baseline visit and follow-up visits, patients will undergo an MRI of the brain and the spinal cord and assessments of body sway, EDSS, ADL, pain VAS and SF-36 questionnaire. Plasma biomarkers will be assessed from samples obtained through routine blood draw and a monthly falls diary will be provided each visit to be completed once a month.

This study will not assess any specific medicinal product or intervention, and the study will not interfere with that prescribed in clinical practice.

Primary outcome measures

  • Spinal cord magnetization transfer ratio (MTR) [Time frame: Change from baseline up to 2 years]
Secondary outcome measures (10)
  • Spinal cord morphometry. Cross sectional area (CSA) to cover the C1 to C7 vertebral levels. [Time frame: Change from baseline up to 2 years]
  • Spinal cord diffusion image analysis parameters: Fractional Anisotropy (FA), Radial Diffusivity (RD), Axial Diffusivity (AD), Mean Diffusivity (MD) at the cervical levels C1-C5. [Time frame: Change from baseline up to 2 years]
  • Brain diffusion image analysis parameters: Fixel-Based analysis (FBA) (Fiber Density (FD), Fiber cross-section (FC) and combination of FD and FC), Diffusion tensor imaging (DTI) (FA, RD, AD, MD, Markers of severity and markers of evolution). [Time frame: Change from baseline up to 2 years]
  • Body sway amplitude (considering antero-posterior and medio-lateral sway with eyes closed, feet apart; eyes open, feet apart; eyes closed, feet together; eyes open, feet together) [Time frame: Change from baseline up to 2 years]
  • Expanded Disability Status Scale (EDSS) [Time frame: Change from baseline up to 2 years]
  • Activities of Daily Living (ADL) [Time frame: Change from baseline up to 2 years]
  • Pain Visual Analogue Scale (Pain VAS) [Time frame: Change from baseline up to 2 years]
  • Monthly falls [Time frame: Change from baseline up to 2 years]
  • Short Form Health Survey (SF-36) [Time frame: Change from baseline up to 2 years]
  • Plasma biomarkers (NFL, MMP-9, IL-18, MIP-1beta and IL-1Ra) [Time frame: Change from baseline up to 2 years]

Eligibility criteria

Inclusion criteria

  • Women aged 18 years old or older.
  • Diagnosis of X-linked ALD based on genetic testing, altered VLCFA levels, or family history.
  • Willing to undergo annual follow-up visits, including brain and spinal cord MRI scans.
  • Provision of written informed consent.
  • Affiliation or beneficiary of a French social security system or of such a regime.

Exclusion criteria

  • Any condition that in the opinion of the investigator are likely to adversely affect the study participation, interfere with study compliance, or confound the study results.
  • Under treatment or previous treatment with leriglitazone.
  • Pregnant or lactating women.
  • Subjects benefiting from laws aimed at protecting vulnerable adults: subjects being deprived of liberty by judicial or administrative decision, subjects under guardianship.
  • Participation in an interventional clinical trial.

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

France · 1 center
  • Paris Brain Institute (ICM) Centre Hospitalier Universitaire Pitié Salpêtrière — Paris

Identifiers

NCT: NCT06178120 · MT-NH-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗