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Study of Systemic Amyloidosis Presentation and Prognosis



Study of Systemic Amyloidosis Presentation and Prognosis

For Condition: Amyloidosis
Status: Recruiting
Sponsor(s): National Center for Research Resources (NCRR) , Indiana University Cancer Center
Synopsis: OBJECTIVES: I. Analyze prospectively the course of amyloid deposition in patients with primary, secondary, myeloma-associated, and hereditary amyloidosis. II. Determine abnormalities of humoral and delayed-type hypersensitivity in these patients. III. Identify prognostic factors in hereditary amyloidosis and develop tests for genetic defects associated with systemic amyloidosis. IV. Diagnose familial amyloidotic polyneuropathy (FAP) prior to symptom onset. V. Validate the correlation of low serum prealbumin and retinol binding protein levels with amyloidosis in patients with FAP.
Details: PROTOCOL OUTLINE: Patients receive a comprehensive evaluation with an emphasis on identifying prognostic and diagnostic factors. Assessments include gastrointestinal, renal, hematologic, dermatologic, cardiac, and serologic studies. Immunologic studies include antinuclear antibody, latex fixation, and serum and urine electrophoresis. Genetic trees are constructed using detailed family history data; blood and urine samples are routinely collected from relatives. Family members of patients with familial amyloidotic polyneuropathy type II (Indiana type) undergo a flexor retinaculum biopsy of the wrist.
Eligibility:
Study Type:
  Observational, Screening
Minimum Age/Maximum Age: /
Genders: Both
Protocol Entry Criteria: PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- Systemic amyloidosis, i.e.: Primary, myeloma associated Secondary, e.g., associated with the following conditions: Rheumatoid arthritis Inflammatory bowel disease
Total Enrollment: 100

Location and Contact Information:

Overall Study Official:
MerrillBenson,  Study Chair,  Indiana University Cancer Center

Indiana University Cancer Center *Recruiting*
Indianapolis,  Indiana,  46202-5265
United States
Recruiting Merrill  Benson 317-278-3426


Additional Information:
Study ID Numbers:
  NCRR-M01RR00750-0062;  IUSM-831215
Study Start Date: January 1979
Record last reviewed: December 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00004374

Other Amyloidosis Studies:
1. Study of High-Dose Melphalan and Autologous Stem Cell Transplantation in Patients With Primary Light Chain Amyloidosis

2. Study of Systemic Amyloidosis Presentation and Prognosis

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