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Clinical Trials/NCT00001979
NCT00001979RecruitingNot Applicable

Studies of Immunologically-Mediated Kidney Diseases

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)1 site in 1 country2,000 target enrollmentStarted: June 25, 1992Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
2,000
Locations
1
Primary Endpoint
Provision of biospecimens

Study Overview

Brief Summary

Kidney diseases related to the immune system include, nephrotic syndrome, glomerulonephritis, membranous nephropathy, lupus nephritis, and nephritis associated with connective tissue disorders.

This study will allow researchers to admit and follow patients suffering from autoimmune diseases of the kidney. It will attempt to provide information about the causes and specific abnormalities associated with autoimmune kidney disease.

Patients with kidney disease as a result of their immune system, and patients with diseases of the immune system who may later develop kidney disease, will be potential subjects for this study.

Patients will undergo a history and physical examination, and standard laboratory test to more closely understand the causes, signs, symptoms, and responses to medication of these diseases. Based on these evaluations the patients may qualify as candidates for other experimental studies. At any time these patients may be asked to submit blood or urine samples for further research.

Detailed Description

Study Description:

This study evaluates participants with known or suspected immunologically-mediated kidney diseases, including but not limited to nephrotic syndrome, glomerulonephritis, membranous nephropathy, lupus nephritis, and nephritis associated with other systemic or connective tissue disorders. Participants who have immunologically-mediated diseases with potential for kidney disease will be evaluated as well. Studies will include characterization of the clinical and laboratory features of these disorders, studies of natural history and complications, evaluation of responses to standard treatment. Blood and urine samples will be collected for immunological research conducted under this protocol.

Objectives:

Primary:

-To collect samples and data obtained during standard clinical care that can be used to better understand rare forms of immunologically-mediated renal disorders, atypical renal disease that have not been fully characterized, and to allow for future research studies.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
10 Years to 99 Years (Child, Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • INCLUSION CRITERIA:
  • In order to be eligible to participate in this study, a participant must meet all of the following criteria:
  • Adults >= 18 years of age and children 10-17 years of age
  • Participants with
  • known, proven, or suspected immunologically-mediated kidney diseases, including but not limited to nephrotic syndrome, glomerulonephritis, membranous nephropathy, lupus nephritis, and nephritis associated with other systemic or connective tissue disorders, OR
  • immunologically-mediated diseases with the potential for kidney disease.
  • Ability of the participant or guardian to understand and the willingness of the participant or guardian to provide written informed consent.

Exclusion Criteria

  • An individual who meets any of the following criteria will be excluded from participation in this study:
  • Concomitant medical problems which would confound the interpretation of studies of the immunologic kidney disorder.
  • Concomitant medical, surgical, or other conditions for which inadequate facilities or funds are available to support their care at the NIH.

Arms & Interventions

Patients

Patients with known or suspected immunologically-mediated kidney diseases or immunologically-mediated diseases with potential for kidney disease.

Outcomes

Primary Outcomes

Provision of biospecimens

Time Frame: ongoing

Patients with autoimmune diseases for whom there are no current experimental treatment protocols can be admitted for study and follow-up; they will provide a ready pool of candidates who can be asked to provide blood specimens for ongoing laboratory studies.

Secondary Outcomes

No secondary outcomes reported

Investigators

Study Sites (1)

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