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Clinical Study and Gene Mutation Analysis of Adrenoleukodystrophy in Taiwanese Children

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ClinicalTrials.gov Identifier: NCT00278044
Recruitment Status : Unknown
Verified January 2006 by Far Eastern Memorial Hospital.
Recruitment status was:  Recruiting
First Posted : January 18, 2006
Last Update Posted : February 9, 2009
Information provided by:

Study Description
Brief Summary:
Study the clinical manifestations and gene mutation of Taiwanese ALD patients

Condition or disease Intervention/treatment
Adrenoleukodystrophy Procedure: blood sampling and medical records

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 20 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Clinical Study and Gene Mutation Analysis of Adrenoleukodystrophy in Taiwanese Children
Study Start Date : January 2006
Estimated Study Completion Date : July 2007

Arms and Interventions

Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • X-ALD patients and family

Exclusion Criteria:

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00278044

Contact: jao shwann liang, MD 02-89667000 ext 4448 j580414@yahoo.com.tw

Far Eastern Memorial Hospital Recruiting
Taipei, Taiwan, 220
Contact: Jao Shwann Liang, MD    02-8966-7000 ext 4448    j580414@yahoo.com.tw   
Sponsors and Collaborators
Far Eastern Memorial Hospital
National Taiwan University Hospital
Fu Jen Catholic University
Principal Investigator: Jao Shwann Liang, MD Far Eastern Memorial Hospital
More Information

ClinicalTrials.gov Identifier: NCT00278044     History of Changes
Other Study ID Numbers: 94028
First Posted: January 18, 2006    Key Record Dates
Last Update Posted: February 9, 2009
Last Verified: January 2006

Keywords provided by Far Eastern Memorial Hospital:
Search as text words in Annotation & Scope Note

Additional relevant MeSH terms:
Brain Diseases, Metabolic, Inborn
Brain Diseases, Metabolic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Hereditary Central Nervous System Demyelinating Diseases
Demyelinating Diseases
Mental Retardation, X-Linked
Intellectual Disability
Neurobehavioral Manifestations
Neurologic Manifestations
Genetic Diseases, X-Linked
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Metabolism, Inborn Errors
Peroxisomal Disorders
Metabolic Diseases
Adrenal Insufficiency
Adrenal Gland Diseases
Endocrine System Diseases