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Completed

NCT Number: NCT02405026

Determine the Prevalence and Severity of Asthma in HIV (Human Immunodeficiency Virus) Infected Patients

The purpose of this study is to determine the prevalence and severity of asthma in patients with HIV. To determine the immunological phenotype of HIV-infected patients with asthma.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Duke Asthma Allergy and Airway Center

Durham, North Carolina, 27705, United States

About this study

Prospectively clinically phenotype and the prevalence of asthma in HIV infected patients in the Duke ID Clinic

  • HIV infected asthmatic subjects meeting clinical definitions for asthma compared to HIV uninfected asthma subjects identified at the DAAAC and HIV infected non-asthmatic subjects.
  • Prospective immunological phenotyping - HIV-infected asthma subjects prospectively identified and clinically phenotyped compared to HIV-uninfected asthma subjects identified at the DAAAC and HIV infected non-asthma subjects.

Regarding the sampling method of probability sample: All samples for HIV infected asthmatic patients, HIV uninfected asthmatic patients and HIV infected non-asthmatics patients will be analyzed.

Retrospectively determine overall asthma prevalence and severity among HIV-infected patients. Retrospective immunological phenotyping (circulating cytokines) of HIV-infected patients utilizing available specimens in the Duke HIV Specimen Biorepository

  • HIV-infected asthmatic subjects meeting asthma definition compared to overall asthma prevalence in U.S. population
  • HIV-infected asthma subjects meeting asthma definitions compared to matched HIV-infected non-asthma subjects

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV infected asthmatic and non-asthmatic adults ≥18 years
  • HIV uninfected asthma adults ≥18 years
  • Females of childbearing potential have to be using medically acceptable contraceptive method for the duration of the study.
  • Willing and able to give informed consent and adhere to visit/protocol schedules.
  • Negative pregnancy test in women of childbearing potential
  • For asthma patients: known or possible diagnosis of asthma for at least one year

Exclusion criteria

  • Antibiotic administration for upper respiratory infection within the prior 30 days
  • Greater than 10 pack a year smoking history
  • No prior use of steroids (systemic) within the past 3 months
  • Underlying illnesses that may result in altered lung function
  • Students or employees who are under direct supervision of any Project or Core PI/Director.
  • Pregnant or nursing mothers.
  • Poorly controlled concomitant conditions as determined by the investigator.
  • Subjects who have had an elective procedure (for example, colonoscopy, cystoscopy, etc.) within less than 2 weeks of the procedure date cannot be enrolled in the HIV Asthma study
  • Subjects must delay enrollment by 2 weeks into the HIV Asthma study if they have received a single dose of systemic steroids

Treatment and study plan

Primary outcomes

  1. Asthma prevalence of HIV infected subjects currently followed at the Duke Infectious Disease (ID) Clinic compared to HIV uninfected asthma subjects identified at the Duke Asthma, Allergy and Airway Center (DAAAC).

    Time frame: 12 months

    Assessed through Asthma control questionnaire, pulse oximetry, FeNO, Spirometry, Methacholine challenge, Induced sputum for differential, serum periostin, questionnaires

  2. Asthma phenotypic characteristics of HIV infected subjects compared to HIV uninfected asthma subjects and HIV infected non-asthmatic subjects.

    Time frame: 12 months

    Assessed through blood collection

Secondary outcomes

  1. Prospective immunological phenotyping of Th1/Th2/Th17 cytokines and T cell subsets

    Time frame: 12 months

    Assessed through blood sample collection

  2. Retrospective immunological phenotyping (circulating cytokines) of HIV-infected patients utilizing available specimens in the Duke HIV Biorepository

    Time frame: 12 months

    The primary measure of is the quantitative difference in IL-6 between HIV-infected asthmatic subjects and HIV-infected non-asthmatic subjects.

  3. Retrospectively determine overall asthma prevalence among HIV-infected patients

    Time frame: 12 months

    HIV-infected asthmatic subjects meeting electronic health records asthma definition Compared overall asthma prevalence in U.S. population.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

HIV and Asthma in the Post-ART (Antiretroviral Therapy) Era

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Apr 1, 2015
Registry last updated
Oct 3, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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