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NCT02627872Active, not recruiting

Clinical & Systems Medicine Investigations of Smoking-related Chronic Obstructive Pulmonary Disease

Source: ClinicalTrials.gov · Last updated 28 Mar 2025

Brief summary (registry, in English)

Chronic Obstructive Pulmonary Disease (COPD) is an increasing global health problem, which primarily increases among the female population. The purpose of this study is to perform in-depth clinical and molecular characterizations of early stage COPD patients, as well as healthy never-smoker and at-risk smoking control populations to identify molecularly related subgroups patients, including gender-related sub-phenotypes of COPD.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
120 (actual)
First submitted
9 Dec 2015
Start date
1 Mar 2007
Primary completion date
31 Dec 2021
Lead sponsor
Karolinska Institutet
Diseases
COPD
NCT number
NCT02627872

What you commit to

  • Study type: Observational
  • Participants enrolled: 120
  • From 1 Mar 2007 to the primary completion date, 31 Dec 2021
  • 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

  • Received antibiotics for a COPD exacerbation in the 3 months prior to study entry
  • Treatment with oral or inhaled glucocorticoids within past 3 months prior to study entry

Other illness

  • Other lung diseases
  • Significant ischaemic heart disease or arrhythmia

Other

  • Atopy (defined as positive specific IgE test)
  • Asthma

Who the study is looking for

  • For smokers, at least 10 pack-years of cigarette smoking
  • For smokers, at least 10 cigarettes/day the past 6 months before study entry Spirometry that meets stage I-II of the Global Initiative for Chronic Obstructive Lung Disease (GOLD) stages (postbronchodilator forced expiratory volume in 1 second (FEV1) of 50%-100% of predicted level and FEV1/forced vital capacity \[FEV1/FVC\] less than 0.7) or normal (postbronchodilator FEV1 greater than 80% of predicted level and forced expiratory volume in 1 second/forced vital capacity \[FEV1/FVC\] greater than 0.7)

Age in the registry: 45 years to 65 years · Sex: All · Accepts 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
Karolinska Institutet/Karolinska University Hospital Solna
Coordinator of this site? Confirm its status
StockholmSwedenUnknown status

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