Participation in a Research Registry for Immune Disorders
| Status: | Recruiting |
|---|---|
| Conditions: | Other Indications, Infectious Disease, HIV / AIDS |
| Therapuetic Areas: | Immunology / Infectious Diseases, Other |
| Healthy: | No |
| Age Range: | Any - 127 |
| Updated: | 2/9/2019 |
| Start Date: | September 30, 2013 |
| End Date: | May 1, 2020 |
| Contact: | Elizabeth K Garabedian, R.N. |
| Email: | garabede@mail.nih.gov |
| Phone: | (301) 435-2443 |
NIH Participation to USIDNET Registry
Background:
- People with primary immune deficiency diseases (PIDD) have weak immune systems. This makes
it hard for their bodies to fight infection. The Immune Deficiency Foundation has a network
to collect data about people with PIDD. It is called the United States Immunodeficiency
Network. It will help doctors and scientists better understand these disorders. The goal is
to get medical data for everyone with these disorders in the U.S. and Canada. Data will be
stored in a registry. Researchers can use it to study if these disorders are increasing. They
can also learn how the disorders are diagnosed and treated.
Objectives:
- To collect data on people with primary immune deficiency disorders.
Eligibility:
- People who have a PIDD.
Design:
- Data can be added with no record of personal identity.
- Data can be added with identity kept separate. This data will be linked to the registry
by a code number.
- Data for the registry includes:
- Family history
- Disease treatment
- Disease characteristics
- Medical history
- Laboratory data
- People with primary immune deficiency diseases (PIDD) have weak immune systems. This makes
it hard for their bodies to fight infection. The Immune Deficiency Foundation has a network
to collect data about people with PIDD. It is called the United States Immunodeficiency
Network. It will help doctors and scientists better understand these disorders. The goal is
to get medical data for everyone with these disorders in the U.S. and Canada. Data will be
stored in a registry. Researchers can use it to study if these disorders are increasing. They
can also learn how the disorders are diagnosed and treated.
Objectives:
- To collect data on people with primary immune deficiency disorders.
Eligibility:
- People who have a PIDD.
Design:
- Data can be added with no record of personal identity.
- Data can be added with identity kept separate. This data will be linked to the registry
by a code number.
- Data for the registry includes:
- Family history
- Disease treatment
- Disease characteristics
- Medical history
- Laboratory data
The purpose of this protocol is to provide a resource for clinical and laboratory research
through enrollment of known immunodeficiency patients into a national registry, the US
Immunodeficiency Network (USIDNET). The registry data will expand NIH s and the nation s
knowledge base about immune deficiency disorders and genetic mutations that lead to these
disorders. Additional registrants from NIH protocols will not only increase the understanding
of the molecular basis of these disorders, but also will serve to document and track the
incidence and progression of complications.
Objectives and specific aims
The purpose of this proposal is to create a mechanism for depositing NIH data into USIDNET.
The patient Registry is designed to obtain longitudinal data on a large number of patients
with primary immunodeficiency diseases, and genetic carriers of these defects in order to:
- Learn more about the phenotypic variations seen in a large number of individual patients
with the same rare molecular diagnosis.
- Determine the natural history of these genetic disorders of immunity and establish
genotype-phenotype correlations.
- Learn effects of various treatment protocols used in these patients over time, including
unexpected side effects that may be unique to a particular diagnostic group.
- To evaluate quality of life using standard tools and correlate these with genotype and
treatment history.
- To promote collaborative research amongst interested investigators by identifying a
larger pool of potential research subjects than would be available at their own
institutions
- To identify patients with a specific diagnosis for potential participation in
multi-institutional clinical trials designed for diagnosis or therapy or their specific
disease.
through enrollment of known immunodeficiency patients into a national registry, the US
Immunodeficiency Network (USIDNET). The registry data will expand NIH s and the nation s
knowledge base about immune deficiency disorders and genetic mutations that lead to these
disorders. Additional registrants from NIH protocols will not only increase the understanding
of the molecular basis of these disorders, but also will serve to document and track the
incidence and progression of complications.
Objectives and specific aims
The purpose of this proposal is to create a mechanism for depositing NIH data into USIDNET.
The patient Registry is designed to obtain longitudinal data on a large number of patients
with primary immunodeficiency diseases, and genetic carriers of these defects in order to:
- Learn more about the phenotypic variations seen in a large number of individual patients
with the same rare molecular diagnosis.
- Determine the natural history of these genetic disorders of immunity and establish
genotype-phenotype correlations.
- Learn effects of various treatment protocols used in these patients over time, including
unexpected side effects that may be unique to a particular diagnostic group.
- To evaluate quality of life using standard tools and correlate these with genotype and
treatment history.
- To promote collaborative research amongst interested investigators by identifying a
larger pool of potential research subjects than would be available at their own
institutions
- To identify patients with a specific diagnosis for potential participation in
multi-institutional clinical trials designed for diagnosis or therapy or their specific
disease.
- INCLUSION CRITERIA
Individuals of all ages, gender, and races with an immunodeficiency disorder from NIH
studies will be accepted for registration. No healthy volunteers will be enrolled.
EXCLUSION CRITERIA
Individuals with immunodeficiency associated with HIV infection, chemotherapy or other
immunosuppressive therapies will not be accepted for registration unless there is clear
evidence that these individuals also have a genetically determined immunodeficiency disease
as well. Adult individuals who do not give informed consent will also be excluded.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
Phone: 800-411-1222
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