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Treatment of the Cholesterol Defect in Smith-Lemli-Opitz Syndrome
This study is enrolling participants by invitation only.
Study NCT00272844   Information provided by Children's Hospital Boston
First Received: January 4, 2006   Last Updated: December 11, 2007   History of Changes

January 4, 2006
December 11, 2007
January 1998
 
Improvement in sterol levels monitored q.3-6 months [ Time Frame: q. 3-6 months over 20+ years ] [ Designated as safety issue: No ]
Improvement in sterol levels monitored q.3-6 months
Complete list of historical versions of study NCT00272844 on ClinicalTrials.gov Archive Site
  • Improved general health, growth, and behavior [ Time Frame: q. 3-6 months over 20 years ] [ Designated as safety issue: Yes ]
  • Improved neuropsychological development [ Time Frame: q. 3-6 months over 20+ years ] [ Designated as safety issue: No ]
  • Improved general health, growth, and behavior
  • Improved neuropsychological development
  • Improvement in MRS sterol metabolites
 
Treatment of the Cholesterol Defect in Smith-Lemli-Opitz Syndrome
Treatment of the Cholesterol Defect in Smith-Lemli-Opitz Syndrome

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.

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.

Phase I, Phase II
Interventional
Treatment, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study
Smith-Lemli-Opitz Syndrome
Drug: crystalline cholesterol oil-based suspension
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Enrolling by invitation
50
January 2017
 

Inclusion Criteria:

  • Biochemical confirmation of sterol defect associated with Smith-Lemli-Opitz syndrome

Exclusion Criteria:

  • Inability to tolerate crystalline cholesterol
  • Inability to travel to Boston 3-4 times/year based on age
Both
 
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00272844
Mira Irons M.D., Children's Hospital Boston
03-11-189R
Children's Hospital Boston
 
Principal Investigator: Mira Irons, M.D. Children's Hospital Boston
Children's Hospital Boston
September 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP