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Study of Protein Translocation in Patients With Beta-Oxidation Disorders

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ClinicalTrials.gov Identifier: NCT00004348
Recruitment Status : Unknown
Verified January 2000 by Office of Rare Diseases (ORD).
Recruitment status was:  Active, not recruiting
First Posted : October 19, 1999
Last Update Posted : June 24, 2005
Sponsor:
Collaborator:
Washington University School of Medicine
Information provided by:
Office of Rare Diseases (ORD)

October 18, 1999
October 19, 1999
June 24, 2005
September 1995
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No Changes Posted
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Study of Protein Translocation in Patients With Beta-Oxidation Disorders
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OBJECTIVES:

I. Characterize inheritance patterns of mutations in patients with beta-oxidation disorders.

PROTOCOL OUTLINE:

Patients undergo clinical and molecular analysis of beta-oxidation enzyme metabolism. The evaluation includes a urinary metabolite profile, and DNA and familial studies.

Observational
Primary Purpose: Screening
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  • Beta-Oxidation Disorder
  • Peroxisomal Disorders
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
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Same as current
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PROTOCOL ENTRY CRITERIA:

Beta-oxidation disorder, including: Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency Very-long-chain acyl-coenzyme A dehydrogenase deficiency Short-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency Long-chain 3-ketoacyl-coenzyme A thiolase deficiency Trifunctional protein deficiency Patient age: 1 day and over

Sexes Eligible for Study: All
Child, Adult, Senior
No
Contact information is only displayed when the study is recruiting subjects
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NCT00004348
199/11907
WUSM-880075R
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Washington University School of Medicine
Study Chair: Arnold W. Strauss Washington University School of Medicine
Office of Rare Diseases (ORD)
January 2000