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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03190837
Other study ID # Pro00081246
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 12, 2017
Est. completion date January 2027

Study information

Verified date August 2023
Source Duke University
Contact Janet Blount
Phone 919-681-7962
Email janet.blount@duke.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study aims are to: a) identify the long-term natural history of Gaucher disease, b) evaluate long-term treatment efficacy of enzyme replacement therapy (ERT) and substrate reduction therapy (SRT), and c) identify potential long-term complications of this disorder. These aims will be accomplished through long-term record review of individuals with all three types of Gaucher disease.


Description:

The study aims (aims a-c) will be accomplished by the systematic monitoring of health records. Health information will be extracted from medical records for patients followed at Duke. Medical records will be requested from treating physicians outside of Duke. The PI, (Dr. Kishnani) a recognized expert in Gaucher disease, is a consultant to the treating physician of virtually all subjects in this study. Subject health status will be monitored at least on an annual basis and as regularly as the medical information is obtained from the treating physician. Enrollment in this study will not alter the standard of care treatment for patients with Gaucher disease.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date January 2027
Est. primary completion date January 2027
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Diagnosis of Gaucher Disease Exclusion Criteria: - Not meeting Inclusion criteria

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Document effects of Gaucher disease in different systems of body, including nervous system, liver, and spleen. Use Gaucher patient's natural histories to understand effects of Gaucher Disease long term. 10 years
Secondary Document adverse events subjects experience on enzyme replacement therapy Use Gaucher patient's therapy history to understand effects of enzyme replacement therapy long term. 10 years
Secondary Document adverse events of subjects on substrate reduction therapy Use Gaucher patient's therapy history to understand effects of substrate reduction therapy long term. 10 years
Secondary Document long-term complications in Gaucher Disease. Use Gaucher patient's natural histories to understand long-term complications of Gaucher Disease. 10 years
Secondary Change in 36-Item Short Form Survey (SF-36) collected every 6 months/1 year. We will use the SF-36 that will be collected every 6 months to 1 year to assess quality-of-life in Gaucher patients. 10 years
Secondary Change in Small Fiber Neuropathy Screening List (SFNSL) collected every 6 months/1 year. The investigators will use the Small Fiber Neuropathy Screening List every 6 months to 1 year to monitor small fiber neuropathy symptoms in Gaucher patients. 10 years
Secondary Document number of subjects experiencing neurological symptoms related to Gaucher, by using Neurological Follow-up exam The investigators will use the Neurological follow-up exam, that will be performed at return visit and every 6 months to 1 year afterward, to screen patients for neurological symptoms related to Gaucher Disease. 10 years
Secondary Change in Parkinson's checklist collected every 6 months/1 year. The investigators will use the Parkinson's checklist that will be collected every 6 months to 1 year to screen patients for Parkinson's symptoms potentially related to Gaucher Disease. 10 years
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