Detection and Characterization of Infections and Infection Susceptibility

Launched by NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES (NIAID) · Nov 28, 2006

Keywords

ClinConnect Summary

This clinical trial is looking into why some people have problems with their immune system, particularly those that make them more likely to get infections. The study aims to improve how we diagnose and treat these immune disorders. If you're an adult or a child over one month old who has been diagnosed with or suspected of having an increased risk of infections, you may be eligible to participate. Family members who are healthy may also join the study. Participants will need to visit the NIH twice, where they will undergo various tests like blood and urine tests, physical exams, and possibly imaging studies like X-rays or MRIs to help researchers understand more about their condition.

Participants should know that while the first visit's travel expenses aren't covered, any follow-up visits may be. There are financial assessments available to check if you qualify for assistance. It’s important to mention that this study doesn’t enroll children younger than two years old or pregnant individuals. Additionally, consent from participants or their guardians will be required for all procedures, and participants will be asked to allow researchers to access their medical records. This study is open to all genders and does not limit participants based on race or disability.

Gender

ALL

Eligibility criteria

• * INCLUSION CRITERIA:
• PATIENTS:
• • Patients known to have, or suspected of having an infection susceptibility and their healthy blood relatives will be eligible for enrollment.
• • Participants must be over 1 month of age. There will be no limit as to sex, race or disability.
• • Patients must have a primary physician outside of the NIH and may be required to submit a letter from their physician that documents their relevant health history.
• • The participant or the participant's guardian will be willing and capable of providing informed consent after initial counseling by clinical staff. Separate consent forms for all interventional procedures will be obtained after explanation of the specific procedure.
• • Patients and relatives must agree to have blood and tissue stored for future studies of the immune system and/or other medical conditions.
• • Patients and relatives may be concurrently enrolled on other protocols as long as the Principal Investigator is informed.
• • The patient must be enrolled on this protocol to have relatives enrolled.
• The patient and patient relative cohorts will include the following special populations:
• • Children: Children are included in this study because immune defects may present in early childhood, and early diagnosis or characterization may benefit subjects. Children who do not meet the age and weight criteria for care at the Clinical Center, may have sample collection only.
• • Decisionally impaired adults: Patients and patient relatives will be able to provide informed consent for themselves or, if they lack the capacity to provide informed consent, the study team will obtain consent from the legally authorized representative. Patients with underlying immune disorders, autoimmune phenomena or severe infections may sometimes present with delirium, encephalopathy, or coma and are therefore unable to provide informed consent. Excluding patients who are unable to provide consent could adversely impact patient access to medical therapy at the NIH as well as adversely impact research recruitment. Excluding patients unable to provide consent would also essentially prohibit us from evaluating patients at higher risk for adverse outcomes and therefore skew our understanding of disease. Similarly, enrolled patient subjects who lose the ability to provide ongoing consent during study participation may continue in the study. The risks and benefits of participation for subjects unable to consent should be identical to those described for less vulnerable patients.
• EXCLUSION CRITERIA:
• • 1. A well understood acquired abnormality which leads to infection susceptibility, such as HIV, cytotoxic chemotherapy, or active malignancy may be adequate explanation for the infection diathesis. These may be grounds for exclusion if, in the opinion of the investigators, the presence of such disease process interferes significantly with evaluation (applicable to patients and their blood relatives).
• • 2. Severe or uncommon infections or syndromes often require highly specialized teams and institutions. Some referred cases will not be able to be handled appropriately at the NIH and may be deemed ineligible for admission, as determined by the Principal Investigator.
• • 3. Pregnancy