Clinical Trial Finder

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  INCLUSION CRITERIA:

  In order to be eligible to participate in this study, an individual must meet all of the following criteria: - Aged 3 to 100 years.

• - a) Suspected or confirmed allergic, atopic, respiratory, or nasal/sinus disorder or have suspected or confirmed history of an immune dysregulatory disorder, OR.

b) Have a clinical history of an immediate hypersensitivity reaction to aeroallergens, food, insect stings, or medications.

• - Able to provide informed consent.

• - Have or are willing to obtain a non-NIH primary physician who will manage all health conditions and be responsive for emergency medical treatment, if required.

• - Willing to allow storage of blood, skin swabs, nasal fluid/brushings, bodily fluids, and other clinically appropriate tissue specimens or data generated during participation for future use in medical research.

EXCLUSION CRITERIA:

An individual who meets any of the following criteria will be excluded from participation in this study:

• - Any condition(s) or diagnosis, physical and/or psychological, that the investigator feels precludes the patient from participation in the study.

--a. Participants who are pregnant.

• - For additional skin biopsies only: - a.

Individuals who have a history of keloid formation.

• - b.

Children (<18 years old)

• - c.

Participants who are pregnant.

• - For additional nasal-sinus polyp biopsies only: - a.

Individuals on blood thinners unless they have already been stopped for the procedure.

• - b.

Children (<18 years old)

• - c.

Participants who are pregnant.

• - For skin prick testing.

--a. Participants who are pregnant.

• - Endoscopic Biopsy.

• - a.

Uncontrolled asthma or Grade 3 or higher by the American Society of Anesthesiologist s Physical Status Classification System.(https://www.asahq.org/standards-and-practice-parameters/statement-on-asaphysical-status- classification-system)

• - b.

History of adverse reaction to conscious sedation or general anesthesia required for endoscopy.

• - c.

Hemoglobin < 11 g/dL.

• - d.

Platelet count < 100,000 microL.

• - e.

Pregnant or breastfeeding.

• - f.

Severe hypoxemia due to chronic pulmonary disease.

• - g.

Recent abdominal surgery.

• - h.

Anticoagulant therapy that cannot be interrupted.

• - i.

Younger than 18 years of age.Participants will be selected in an equitable manner from the available pool of potentially eligible individuals, without regard to factors such as sex, gender, race, ethnicity, sexual orientation, or socioeconomic status.

Study Description: This is a single-site repository study that will prospectively collect samples and data from participants with allergic and atopic diseases and associated conditions such as chronic rhinosinusitis and nasal polyposis, through the evaluation, testing, and monitoring of patients with these conditions at the NIH Clinical Center (CC) and via telehealth visits and/or send-in samples. This repository will provide atopic participant samples for translational studies performed by NIH investigators or their collaborators and also serve as a means for recruiting atopic control patients to ongoing NIAID and National Institute on Deafness and Other Communication Disorders (NIDCD) clinical studies. Participants aged 3 and older will present to the NIH CC for visits for clinical evaluation and treatment of allergic diseases as appropriate. Data and samples obtained but not utilized from clinically indicated procedures will be put into the repository (e.g. physical exams, nasal endoscopy, blood tests, olfaction assessment, and nasal sinus polyp biopsy where appropriate). Samples that may be collected prospectively for inclusion in the repository include nasal brushings, nasal lining fluid, blood, urine, and skin swabs. Additionally, extra skin, nasal sinus polyp, and gastrointestinal biopsies may be collected during clinically indicated procedures. The following assessments will also be performed for research purposes: Data collected from patient reported outcomes (PROs) and questionnaires, blood, urine, allergy skin prick testing, skin swab, and pulmonary function testing to include fractional exhaled nitric oxide testing (FeNO). Data/samples from clinical procedures will also be collected for the repository, where possible. Although standard of care treatment may be initiated and monitored under this protocol, it will be expected that after a set number of visits outlined in the manual of operations, continued medication prescribing and monitoring will be transitioned to the referring provider, the patient s outside primary physician or allergist-immunologist, or another NIH protocol depending on the patient condition and importance for biorepository collection. No experimental treatments will be offered under this protocol. Objective: To create a repository of clinical, laboratory, and diagnostic data and specimens from a cohort of suspected or confirmed atopic or allergic individuals with diverse disorders seen by allergist-immunologists and rhinologists.

Arms

: Conditions that may be initially evaluated or managed by A&amp;I but not categorized in 1 or 2 above

Conditions that may be initially evaluated or managed by an allergist-immunologist or rhinologist but not categorized in (1) or (2) above (eg, hypereosinophilia, mast cell disorders, pruritus, chronic cough, smell disorders)

: Individuals with a suspected allergic or atopic disease

Individuals with a suspected allergic or atopic disease, but without demonstrated allergen sensitization (eg, contact hypersensitivity, chronic spontaneous urticaria, drug allergy)

: Individuals with an allergic, atopic, or sinus disease

Individuals with an allergic, atopic, or sinus disease (eg, atopic dermatitis, eosinophilic esophagitis (EoE), asthma, chronic rhinosinusitis with polyposis) with documented allergen sensitization in the skin or blood

Interventions