Viewing Study NCT00004350


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Study NCT ID: NCT00004350
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 1999-10-18
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Evaluation of Fanconi Syndrome and Cystinosis
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003554', 'term': 'Cystinosis'}, {'id': 'D005198', 'term': 'Fanconi Syndrome'}, {'id': 'D035583', 'term': 'Rare Diseases'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}], 'ancestors': [{'id': 'D016464', 'term': 'Lysosomal Storage Diseases'}, {'id': 'D008661', 'term': 'Metabolism, Inborn Errors'}, {'id': 'D030342', 'term': 'Genetic Diseases, Inborn'}, {'id': 'D009358', 'term': 'Congenital, Hereditary, and Neonatal Diseases and Abnormalities'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}, {'id': 'D015499', 'term': 'Renal Tubular Transport, Inborn Errors'}, {'id': 'D007674', 'term': 'Kidney Diseases'}, {'id': 'D014570', 'term': 'Urologic Diseases'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D052801', 'term': 'Male Urogenital Diseases'}, {'id': 'D020969', 'term': 'Disease Attributes'}, {'id': 'D010335', 'term': 'Pathologic Processes'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'enrollmentInfo': {'count': 12}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '1999-10'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '1999-12', 'lastUpdateSubmitDate': '2005-06-23', 'studyFirstSubmitDate': '1999-10-18', 'studyFirstSubmitQcDate': '1999-10-18', 'lastUpdatePostDateStruct': {'date': '2005-06-24', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '1999-10-19', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['Fanconi syndrome', 'cystinosis', 'rare disease', 'renal and genitourinary disorders'], 'conditions': ['Cystinosis', 'Fanconi Syndrome']}, 'descriptionModule': {'briefSummary': 'OBJECTIVES:\n\nI. Classify renal tubular defects using clinical and biochemical findings in patients with Fanconi syndrome and cystinosis.', 'detailedDescription': 'PROTOCOL OUTLINE:\n\nPatients receive a clinical and biochemical evaluation, including a psychometric assessment and molecular, renal, and thyroid studies.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT', 'OLDER_ADULT'], 'minimumAge': '0 Years', 'healthyVolunteers': False, 'eligibilityCriteria': '* Inherited renal tubular defects, i.e., Fanconi syndrome\n* Fanconi syndrome due to cystinosis eligible'}, 'identificationModule': {'nctId': 'NCT00004350', 'briefTitle': 'Evaluation of Fanconi Syndrome and Cystinosis', 'organization': {'class': 'NIH', 'fullName': 'Office of Rare Diseases (ORD)'}, 'orgStudyIdInfo': {'id': '199/11911'}, 'secondaryIdInfos': [{'id': 'UCSD-012'}]}, 'contactsLocationsModule': {'overallOfficials': [{'name': 'Jerry A. Schneider', 'role': 'STUDY_CHAIR', 'affiliation': 'University of California, San Diego'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'National Center for Research Resources (NCRR)', 'class': 'NIH'}, 'collaborators': [{'name': 'University of California, San Diego', 'class': 'OTHER'}]}}}