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NCT02836067Completed

Impact of Smoking and Its Cessation on Systemic and Airway Immune Activation

Source: ClinicalTrials.gov · Last updated 5 Jan 2024

Brief summary (registry, in English)

The purpose of this study is to learn how smoking affects the immune systems in people with HIV infection. The investigators would like to know if HIV infected smokers who quit smoking have different responses in their tissues from people who keep smoking.

Status (registry)
Completed
Study type
Interventional
Enrollment
53 (actual)
First submitted
14 Jul 2016
Start date
15 Jun 2017
Primary completion date
31 Dec 2023
Lead sponsor
Boston Medical Center
Diseases
HIV
NCT number
NCT02836067

What you commit to

  • Study type: Interventional
  • Participants enrolled: 53
  • From 15 Jun 2017 to the primary completion date, 31 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Active malignancy and receiving concurrent treatment (i.e. chemotherapy, radiation therapy, investigational treatment).
  • Self-reported regular use of inhaled substances (such as crack, fentanyl, heroin, hookah, e-cigarettes) in the past (prior to 1 month ago and within the past 5 years), with use occurring for \> 1 year. (Marijuana use is allowable.)
  • A history of alcohol dependence within the 6 months prior to enrollment
  • Currently taking anticoagulants including but not limited to: heparin (Hep-Lock, Hep-Pak), Hep-Pak CVC, Heparin Lock Flush), warfarin (Coumadin), tinzaparin (Innohep), enoxaparin (Lovenox), danaparoid (Orgaran), dalteparin (Fragmin), clopidogrel (Plavix), prophylactic aspirin, and NSAID use and unable to stop for 48 hours prior to bronchoscopy
  • Taking any of the following medications within 30 days prior to enrollment: systemic steroids (inhaled or nasal steroid therapy is permitted), interleukins, systemic interferons (e.g., local injection of interferon alpha for treatment of HPV is permitted) or systemic chemotherapy, anti-TNF agents
  • Recent abdominal surgery (within past 3 months)
  • Recent eye surgery (within past 3 months)

Other illness

  • Significant immunological illnesses/deficiencies
  • Recent active illness within the past 1 month (i.e. respiratory viral infection, pneumonia, bacterial infections, bone infection)
  • History of tuberculosis, lung cancer, bronchiectasis, pulmonary fibrosis, or pulmonary hypertension
  • History of intolerance, sensitivity, allergy or anaphylaxis to lidocaine or other amide anesthetics, as well as benzocaine or other ester type anesthetics
  • History of recent myocardial infarction (within past 6 months). Non-coronary ischemia MI is allowed (i.e. cocaine-induced)
  • Chronic renal failure requiring dialysis

Other

  • Pregnant or breast-feeding or less than 8 weeks post-partum.
  • Self-reported regular or recreational use of inhaled substances (such as marijuana, crack, fentanyl, heroin, hookah, e-cigarettes) as well as chewing tobacco within past month. Reports of no such use within the past month will be confirmed by a urine tox screen performed at the Screening Visit.
  • Spirometry criteria FEV1/FVC \< 0.7 (definition of COPD) and GOLD (severe-very severe) Stage 3 or 4 within past 12 months
  • Decompensated cirrhosis
  • Investigator discretion

Who the study is looking for

  • HIV infected on ART ≥ 6 months
  • Virologically suppressed (\<50 cop/ml) at the time of enrollment (lab test within 3 months )
  • Smoking Status:
    • Currently Active Smoker: Self-reported regular cigarette use with positive cotinine test at screening visit.
    • OR Non-smoker: self-reported non-smokers confirmed by negative cotinine test at screening visit.
  • Laboratory values within 3 months prior to enrollment that meet the following criteria:
    • Hemoglobin ≥ 8.0 g/dL
    • Platelet count ≥ 80,000/mm3
  • For females of child-bearing potential: Negative urine pregnancy test (sensitive to 25 IU HCG) at screening visit.
    • For purposes of this study, a female is considered of child-bearing potential unless:
  • Permanently sterile (includes hysterectomy, bilateral oophorectomy, or bilateral salpingectomy)
  • Medically documented ovarian failure
  • Post-menopausal, defined as ≥ 55 years of age with cessation of menses for ≥ 12 months

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Boston Medical Center
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.