Menu
Recruiting NCT03789721

Adrenoleukodystrophy National Registry Study

— Observational ALD (Adrenoleukodystrophy) Adrenoleukodystrophy Cerebral 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
The protocol lists: Medical Record Abstraction, Biospecimen Sample Collection.
Who it may be relevant to
Registry conditions: ALD (Adrenoleukodystrophy), Adrenoleukodystrophy, Cerebral Adrenoleukodystrophy. Basic parameters: No limits · All.
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
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The aim of this registry to understand the natural history and disease progression in ALD and potentially develop bio-markers using the biospecimens collected using this registry.

Detailed description

This is a prospective, non-therapeutic protocol designed to create and maintain a registry of participants with Adrenoleukodystrophy (ALD) and known/presumed mutation for ALD. This study also involves maintaining a prospective biorepository to collect and store buccal swab, blood, stool and urine samples as well. In this protocol, pediatric (including infants), adolescents and adult patients with confirmed or presumed ALD (based on positive VLCFA testing and/or confirmed mutation) will be offered potential study participation. Additionally, presumed mutation for ALD (based on pedigree or confirmed mutation) will be offered potential study participation. After appropriate consent (online or in-person), subjects will be requested to provide a medical history (with authorization of release of medical records), longitudinal biospecimens, and permission to perform laboratory analyses on these samples. The overall goal is to understand the natural disease course in affected and unaffected patients (identified patients and relatives with a diagnosis of ALD), as well as women with ALD to assemble a resource of clinical, medical, and biological data from the participants. This study also aims to understand the outcomes of this disease, as well as possibly develop biomarkers to identify prognostic markers for disease progression, which may help develop effective interventions. The biospecimen bank and registry will provide access to samples and data for the ongoing studies as well as will provide an important resource for the future research.

Interventions

  • Other Medical Record Abstraction
    Collect clinical and epidemiological data through medical record abstraction and self-reported questionnaire survey semi-annually.
  • Other Biospecimen Sample Collection
    Collect research samples, when feasible for those diagnosed with ALD.

Primary outcome measures

  • Collect Clinical and Epidemiological Data [Time frame: 10 Years]

Eligibility criteria

Inclusion criteria

  • Age 0 - 100
  • ALD patients or family member meeting any of the following criteria:
  • Any patient diagnosed with ALD (confirmed by positive VLCFA testing and/or genetic mutation).
  • Known or presumed mutation with ALD based on pedigree or confirmed mutation in ABCD1 gene
  • Participants living in the United States and territories

Exclusion criteria

  • Patients diagnosed with ALD who lack the capacity to consent/assent AND do not have a designated legally authorized representative or guardian.
  • Patients who have undergone BMT or other cellular therapy .
  • Patients not fluent in English who are unable to consent in-person at the BMT Journey Clinic.
  • Patients who are illiterate
  • Patient determined by the PI or designee to be unlikely to complete required study components (due to language barriers, compliance issues, etc.)

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
Cohort

Study locations

United States · 1 center
  • Masonic Cancer Center at University of Minnesota — Minneapolis

Identifiers

NCT: NCT03789721 · 2019NTLS027 · MT2019-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗