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Clinical Study and Gene Mutation Analysis of Adrenoleukodystrophy in Taiwanese Children

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified January 2006 by Far Eastern Memorial Hospital.
Recruitment status was:  Recruiting
National Taiwan University Hospital
Fu Jen Catholic University
Information provided by:
Far Eastern Memorial Hospital Identifier:
First received: January 16, 2006
Last updated: February 6, 2009
Last verified: January 2006
Study the clinical manifestations and gene mutation of Taiwanese ALD patients

Condition Intervention
Procedure: blood sampling and medical records

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Diagnostic
Official Title: Clinical Study and Gene Mutation Analysis of Adrenoleukodystrophy in Taiwanese Children

Resource links provided by NLM:

Further study details as provided by Far Eastern Memorial Hospital:

Estimated Enrollment: 20
Study Start Date: January 2006
Estimated Study Completion Date: July 2007

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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00278044

Contact: jao shwann liang, MD 02-89667000 ext 4448

Far Eastern Memorial Hospital Recruiting
Taipei, Taiwan, 220
Contact: Jao Shwann Liang, MD    02-8966-7000 ext 4448   
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 Identifier: NCT00278044     History of Changes
Other Study ID Numbers: 94028
Study First Received: January 16, 2006
Last Updated: February 6, 2009

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 processed this record on May 24, 2017