- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00004312
Establishment of a Database for Long-Term Monitoring of Patients With Nephropathic Cystinosis
OBJECTIVES: I. Establish a computerized databank to monitor the progress of patients with cystinosis treated with cysteamine.
II. Track and monitor all patients including renal transplant, dialysis and post renal transplants.
Study Overview
Status
Conditions
Detailed Description
PROTOCOL OUTLINE:
Data are collected from patients and physicians. Information includes disease, treatment, family history, demographic, and physical exam data. The dates of kidney transplantation and/or dialysis initiation are also recorded.
Study Type
Enrollment
Contacts and Locations
Study Locations
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California
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La Jolla, California, United States, 92093-0652
- University of California San Diego School of Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
PROTOCOL ENTRY CRITERIA:
Nephropathic cystinosis diagnosis by white-cell cystine measurement, including infantile and late-onset forms
Study Plan
How is the study designed?
Collaborators and Investigators
Collaborators
Investigators
- Study Chair: Jerry A. Schneider, University of California, San Diego
Study record dates
Study Major Dates
Study Start
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NCRR-M01RR00827-1196
- UCSD-970026
- UCSD-950338
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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