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| Tracking Information | |||||
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| First Received Date ICMJE | January 4, 2006 | ||||
| Last Updated Date | December 11, 2007 | ||||
| Start Date ICMJE | January 1998 | ||||
| Primary Completion Date | |||||
| Current Primary Outcome Measures ICMJE |
Improvement in sterol levels monitored q.3-6 months [ Time Frame: q. 3-6 months over 20+ years ] [ Designated as safety issue: No ] | ||||
| Original Primary Outcome Measures ICMJE |
Improvement in sterol levels monitored q.3-6 months | ||||
| Change History | Complete list of historical versions of study NCT00272844 on ClinicalTrials.gov Archive Site | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Descriptive Information | |||||
| Brief Title ICMJE | Treatment of the Cholesterol Defect in Smith-Lemli-Opitz Syndrome | ||||
| Official Title ICMJE | Treatment of the Cholesterol Defect in Smith-Lemli-Opitz Syndrome | ||||
| Brief Summary | The purpose of this study is to determine whether supplementation with an oil-based cholesterol suspension will correct the biochemical abnormalities in cholesterol and its precursors in individuals with the Smith-Lemli-Opitz syndrome. |
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| Detailed Description | This study involves treating individuals with the Smith-Lemli-Opitz syndrome, a rare inborn error of cholesterol metabolism, with supplemental cholesterol to determine it effects on biochemical sterol metabolites, growth, neuropsychological development, ophthalmologic and auditory function, ERG (electroretinogram) parameters, and CNS metabolites as determined by brain MRS-imaging. Safety of the supplemental cholesterol suspension is monitored by tests of hematologic, renal, and liver function at periodic intervals. There is also a substudy that is investigating potential genotype-phenotype correlations, as well as another that studies biochemical parameters of light sensitivity in cultured skin fibroblasts from affected patients. |
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| Study Phase | Phase I, Phase II | ||||
| Study Type ICMJE | Interventional | ||||
| Study Design ICMJE | Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study | ||||
| Condition ICMJE | Smith-Lemli-Opitz Syndrome | ||||
| Intervention ICMJE | Drug: crystalline cholesterol oil-based suspension | ||||
| Study Arms / Comparison Groups | |||||
| Publications * |
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||
| Recruitment Status ICMJE | Enrolling by invitation | ||||
| Estimated Enrollment ICMJE | 50 | ||||
| Estimated Completion Date | January 2017 | ||||
| Primary Completion Date | |||||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both | ||||
| Ages | |||||
| Accepts Healthy Volunteers | No | ||||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | ||||
| Location Countries ICMJE | United States | ||||
| Administrative Information | |||||
| NCT ID ICMJE | NCT00272844 | ||||
| Responsible Party | Mira Irons M.D., Children's Hospital Boston | ||||
| Study ID Numbers ICMJE | 03-11-189R | ||||
| Study Sponsor ICMJE | Children's Hospital Boston | ||||
| Collaborators ICMJE | |||||
| Investigators ICMJE |
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| Information Provided By | Children's Hospital Boston | ||||
| Verification Date | September 2006 | ||||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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