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Evaluation of Fanconi Syndrome and Cystinosis



Evaluation of Fanconi Syndrome and Cystinosis

For Condition: Cystinosis,Fanconi Syndrome
Status: Completed
Sponsor(s): National Center for Research Resources (NCRR) , University of California, San Diego
Synopsis: OBJECTIVES: I. Classify renal tubular defects using clinical and biochemical findings in patients with Fanconi syndrome and cystinosis.
Details: PROTOCOL OUTLINE: Patients receive a clinical and biochemical evaluation, including a psychometric assessment and molecular, renal, and thyroid studies.
Eligibility:
Study Type:
  Observational, Screening
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: - Inherited renal tubular defects, i.e., Fanconi syndrome - Fanconi syndrome due to cystinosis eligible
Total Enrollment: 12

Location and Contact Information:

Overall Study Official:
JerrySchneider,  Study Chair,  University of California, San Diego


Additional Information:
Study ID Numbers:
  199/11911;  UCSD-012
Study Start Date: October 1999
Record last reviewed: December 1999
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00004350

Other Fanconi Syndrome Studies:
1. New Cysteamine Eye Drops Formulation to Treat Corneal Crystals in Cystinosis

2. The Role of Susceptibility to Thrombosis in the Pseudotumor Cerebri of Nephropathic Cystinosis: A Case-Control Study

3. Evaluation of Fanconi Syndrome and Cystinosis

4. Cysteamine Eye Drops to Treat Corneal Crystals in Cystinosis

5. Randomized Study of New Formulation Ophthalmic Cysteamine Hydrochloride for Corneal Cystine Accumulation in Patients With Cystinosis

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