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COPD in Obese Patients

V

Voronezh N.N. Burdenko State Medical Academy

Status

Completed

Conditions

Obese
Obesity, Abdominal
Copd

Study type

Observational

Funder types

Other

Identifiers

NCT04105075
YSShkatova

Details and patient eligibility

About

The study included 176 patients with COPD. The first group included 88 normal weight patients with COPD: 71 men and 17 women, mean age 62.40 ± 8.83 years. The second group included 88 patients with COPD and obesity: 64 men and 24 women, mean age 62.94 ± 5.96 years. We assessed the frequency of COPD exacerbations in last 12 months, the severity of symptoms such as dyspnea, sputum production, fatigue. Spirometry, six-minute walk test and analysis of body tissue type composition were performed. BODE index was calculated. Levels of leptin, adiponectin, interleukins-4,6,8,10, interferon-γ, c-reactive protein (CRP), tumor necrosis factor receptor 1 (TNF-R1), tumor necrosis factor receptor 2 (TNF-R2), tumor necrosis factor alpha (TNF-α) were measured in blood serum.

Enrollment

176 patients

Sex

All

Ages

30 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COPD diagnosis, informed consent for voluntary participation in the study

Exclusion criteria

  • patient participation in any interventional study,
  • COPD exacerbation,
  • concomitant lung diseases, such as confirmed or suspected malignant lung disease or other respiratory disease, such as interstitial pulmonary fibrosis, tuberculosis, sarcoidosis, bronchial asthma, bronchiectasis,
  • concomitant diseases of other organs and systems, such as acute cardiovascular diseases, chronic kidney diseases and liver failure.

Trial design

176 participants in 2 patient groups

Patients with COPD and obesity
Description:
Patients consented to have a blood sample taken
Normal body weight patients with COPD
Description:
Patients consented to have a blood sample taken

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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