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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00004350
Other study ID # 199/11911
Secondary ID UCSD-012
Status Completed
Phase N/A
First received October 18, 1999
Last updated June 23, 2005
Start date October 1999

Study information

Verified date December 1999
Source Office of Rare Diseases (ORD)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Observational

Clinical Trial Summary

OBJECTIVES:

I. Classify renal tubular defects using clinical and biochemical findings in patients with Fanconi syndrome and cystinosis.


Description:

PROTOCOL OUTLINE:

Patients receive a clinical and biochemical evaluation, including a psychometric assessment and molecular, renal, and thyroid studies.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility - Inherited renal tubular defects, i.e., Fanconi syndrome

- Fanconi syndrome due to cystinosis eligible

Study Design

Primary Purpose: Screening


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
National Center for Research Resources (NCRR) University of California, San Diego
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