Skip to main content
Clinical Trials/NCT01884220
NCT01884220
Completed
N/A

A Historical Chart Review and Longitudinal Follow-Up of Identified Patients With Wolman Disease or Cholesteryl Ester Storage Disease, Lysosomal Acid Lipase Deficiency

Children's Hospital Medical Center, Cincinnati1 site in 1 country4 target enrollmentNovember 2010

Overview

Phase
N/A
Intervention
Not specified
Conditions
Wolman Disease
Sponsor
Children's Hospital Medical Center, Cincinnati
Enrollment
4
Locations
1
Primary Endpoint
Change in Organ Measurements using Ultrasound Imaging
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study are: to characterize and understand the natural history of disease progression in WD and CESD, and to provide historical controls for WD and CESD for developing clinical treatment trials. The hypothesis is that the variability and clinical progression in WD and CESD is large and represents a continuum of severities from a lethal infantile to near normal adults with only "fatty livers".

Detailed Description

This is a single institution historical cohort study of patients with Wolman (WD) or Cholesteryl Ester Storage Disease (CESD). Retrospective data will be collected and abstracted from the medical records of both living and deceased patients. Additionally prospective data from living patients will be collected and abstracted annually until the end of the study. Literature sources will be used as secondary source data and will be screened to minimize/eliminate duplicative reports.

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
May 2014
Last Updated
10 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • male or female of any age;
  • a clinical diagnosis of WD or CESD as defined by:
  • documented LAL enzyme deficiency OR
  • LAL gene mutations OR
  • a clinical course and tissue biopsy consistent with CESD or WD;
  • written informed consent

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Change in Organ Measurements using Ultrasound Imaging

Time Frame: Baseline, Year 1, Year 2, Year 3, Year 4

Measurement of the effect over time of LAL deficiency on the liver, spleen, intestines, lungs and adrenals will be performed using ultrasound imaging. Measurement using ultrasound imaging will only be completed if clinically indicated during clinical-care patient visits.

Secondary Outcomes

  • Change in Organ Measurements using X-Ray Imaging(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in Organ Measurements using Computerized Tomography(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in Organ Measurements using Magnetic Resonance Imaging(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in Liver Function using Standardized Laboratory Liver Function Assessment(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in Pulmonary Function using Standardized Pulmonary Function Assessment(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in Subjects's Overall Health Status using Clinical Exam(Baseline, Year 1, Year 2, Year 3, Year 4)
  • Change in the Subject's Overall Health Status using Verbal Report(Baseline, Year 1, Year 2, Year 3, Year 4)

Study Sites (1)

Loading locations...

Similar Trials