Viewing Study NCT00005103



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Last Modification Date: 2024-10-26 @ 9:04 AM
Study NCT ID: NCT00005103
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 2000-04-06

Brief Title: Study of the Pathogenesis of Porphyria Cutanea Tarda
Sponsor: National Center for Research Resources NCRR
Organization: National Center for Research Resources NCRR

Study Overview

Official Title: None
Status: COMPLETED
Status Verified Date: 2003-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: OBJECTIVES I Determine the effect of standard treatments on various predisposing factors in patients with porphyria cutanea tarda PCT

II Investigate alcohol history smoking liver dysfunction and its etiology estrogen use and family history of PCT in these patients

III Study the relationships of excess iron and the hemochromatosis gene to PCT including clinical features and risk of recurrence in these patients

IV Assess hepatitis C virus infections in these patients V Assess vitamin C levels in these patients before and after treatment VI Assess dietary habits in these patients VII Assess activity of cytochrome P450 enzymes CYP in vivo in these patients

VIII Study polymorphic genes for enzymes that metabolize foreign chemicals including CYP enzymes and glutathione transferases in these patients
Detailed Description: PROTOCOL OUTLINE Patients undergo a complete medical evaluation and documentation of porphyria cutanea tarda PCT including history physical examination standard clinical laboratory tests and porphyrin studies Alcohol history smoking liver dysfunction and its etiology estrogen use and family history of PCT are investigated and recorded Patients complete a questionnaire to assess intake of vitamin C and other nutrients

Iron status is assessed by serum ferritin Fe and Fe binding capacity and by the number of phlebotomies needed to reduce ferritin to the target level A blood sample is tested for the hemochromatosis HC gene to determine whether each patient has 0 1 or 2 copies of the HC mutation

Serum hepatitis C virus HCV antibody and HCV RNA are measured Standard liver function tests and liver biopsy are done if clinically indicated

A fasting blood level of ascorbic acid is obtained Blood clearance of caffeine and antipyrine and urinary excretion of caffeine and chlorzoxazone metabolites are determined by breath tests or measurements in blood or saliva

Genotyping for polymorphic genes for enzymes that metabolize foreign chemicals including cytochrome P450 enzymes CYP and glutathione transferases are completed

Following completion of the above studies patients undergo individualized standard treatment either by serial phlebotomies or low dose chloroquine Patients with HCV are also treated with interferon alfa-2b

Patients are followed after treatment at which time initial studies are repeated

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:
Secondary IDs
Secondary ID Type Domain Link
UTMB-95-173 None None None
UTMB-433 None None None