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
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Adrenoleukodystrophy | Procedure: blood sampling and medical records | Not Applicable |
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 |


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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:

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 |
Taiwan | |
Far Eastern Memorial Hospital | Recruiting |
Taipei, Taiwan, 220 | |
Contact: Jao Shwann Liang, MD 02-8966-7000 ext 4448 j580414@yahoo.com.tw |
Principal Investigator: | Jao Shwann Liang, MD | Far Eastern Memorial Hospital |
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:
Adrenoleukodystrophy Brain Diseases, Metabolic, Inborn Brain Diseases, Metabolic Brain Diseases Central Nervous System Diseases Nervous System Diseases Hereditary Central Nervous System Demyelinating Diseases Leukoencephalopathies 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 |