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COPD: Transition of systemic inflammation into multiorgan pathology (study 3).

COPD: Transition of systemic inflammation into multiorgan pathology (study 3). - Multiorgan pathology in COPD

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32013
Enrollment
60
Registered
2008-12-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic obstructive bronchitis ( COPD) emphysema

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Age 40-75 years • Age, pack years, FEV1/FVC and FEV1% predicted must fit in one of 2 groups of table 4.3 • Physically and mentally able to undergo the total study protocol • Written informed consent

Exclusion criteria

Exclusion criteria: • Participation in another study • asthma • Alpha-1-antitrypsin deficiency • Selected within the red made gradation of the 1-3 co-morbidity list in the ACE-27 • Active pulmonary infection like tuberculosis, pneumonia, flue, tracheobronchitis • Active extra-pulmonary infection like hepatitis A-C, cystitis, gastro-enteritis etc • Pulmonary diseases like sarcoidosis, IPF, silicosis, hypersensitivity pneumonitis • Life threatening diseases like carcinoma, AIDS (including HIV+), acute leukaemia etc • Medication that may affect the results of the study: NSAID*s, immunosuppressive agents like prednisolon, metotrexate, azathioprine, sintrom tablets

Design outcomes

Primary

MeasureTime frame
1. Smoking history and behaviour, diet and physical activity level assessed by questionnaire 2. Extensive lung function and CT scanning of the lung 3. Candidate genes for muscle dysfunction and CVD risk 4. Body composition 5. Systemic inflammation 6. Risk factors of metabolic syndrome 7. AGES 8. 6 minute walking distance 9. handgrip strength 10. physical activity level by questionnaire 11. Muscle oxidative phenotype, fibre cross-sectional area and molecular signatures obtained in vastus lateralis muscle biopsies before and after incremental cycly ergometry 12. Skeletal muscle function by isokinetic dynamometry 13. Physical activity level and pattern by accelerometry 14. Glucose tolerance test

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)