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Effects of Electronic Cigarettes in Cigarette Smokers With Mild to Moderate COPD

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Mass General Brigham

Status

Withdrawn

Conditions

COPD
Tobacco Use

Treatments

Other: Electronic cigarette

Study type

Interventional

Funder types

Other

Identifiers

NCT03379025
2017P002418

Details and patient eligibility

About

This study evaluates the effects of electronic cigarette use on cigarette smoking and markers of tobacco use, as well as respiratory symptoms and function in smokers with mild to moderate chronic obstructive pulmonary disease (COPD). All participants will receive a 12 week supply of electronic cigarettes to use instead of their regular conventional cigarettes.

Full description

Electronic cigarettes are devices that heat a solution containing nicotine to form an aerosol that is then inhaled by the user. Electronic cigarettes are used by many smokers, including smokers with chronic health conditions such as COPD. Given that e-cigarettes are still relatively new, their effects on health are not well defined.

It is important to understand how electronic cigarettes affects symptoms and lung function in smokers with COPD to determine the short-term safety of these products. To do this, an initial step involves observing the extent to which smokers substitute their conventional cigarette use with electronic cigarette use and change their exposure to tobacco use biomarkers.

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At least 10 pack year smoking history
  • Daily use of at least 5 cigarettes
  • No plan to quit cigarettes in the next 30 days
  • Willing to use e-cigarettes
  • Diagnosis of COPD (FEV1/forced vital capacity [FVC] <0.70) with mild (FEV1 >80% predicted) or moderate (FEV1 <80% but >50% predicted) airflow limitation (post-bronchodilator); confirmed by spirometry
  • English-speaking

Exclusion criteria

  • Past 30-day use of nicotine-containing products (cigars, cigarillos, hookah, electronic cigarettes, smokeless tobacco, nicotine replacement therapy)
  • Past 30 day use of inhaled drugs (marijuana, crack)
  • Pregnant or breastfeeding
  • Planning to become pregnant within the next 3 months or unable to agree to use appropriate contraception during study
  • Pulmonary disease other than COPD or asthma
  • Ever requiring mechanical ventilation
  • 2 or more hospitalizations for COPD in the past 12 months
  • Cardiac hospitalization in the past 6 months
  • Active chest pain or palpitations
  • Uncontrolled hypertension (blood pressure >160/100)
  • Oxygen therapy
  • Inability or contraindication to perform spirometry (e.g. recent eye, thoracic, or abdominal surgery)
  • Known allergy to propylene glycol or vegetable glycerin
  • Unable to consent or complete assessments

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Early Intervention Group
Experimental group
Description:
JUUL Electronic Cigarettes, nicotine concentration 59 mg/ml, to replace all cigarette use for 12 weeks
Treatment:
Other: Electronic cigarette
Delayed Intervention Group
Other group
Description:
After a 12 week period of no electronic cigarette use, JUUL Electronic Cigarettes, nicotine concentration 59 mg/ml, to replace all cigarette use for 12 weeks
Treatment:
Other: Electronic cigarette

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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