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Osteoporosis and Chronic Obstructive Pulmonary Disease (COPD)

Osteoporosis and COPD (Making of a Database)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00231127
Enrollment
250
Registered
2005-10-04
Start date
2005-04-30
Completion date
2009-01-31
Last updated
2009-11-10

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

Conditions

COPD, Osteopenia, Osteoporosis

Keywords

COPD, Osteoporosis, Osteopenia, Glucocorticoids, GOLD, BODE

Brief summary

The goals of the trial are: * To determine the prevalence of osteoporosis in subgroups of COPD patients. * To look for risk factors of osteoporosis in COPD patients. * To create sub-groups for prospective research concerning the effects of bisphosphonates on osteoporosis variables in COPD patients.

Detailed description

Background: Osteoporosis is defined as a systemically skeletal disorder characterized by a low bone mass and deterioration of the micro-architecture of the bone and is therefore associated with a higher risk of fractures. Large epidemiological studies to determine the incidence and prevalence of osteoporosis in COPD patients in different stages of their disease are not available. The etiology of osteoporosis in COPD patients is complex and depends on multiple factors. Goals of the Trial: * To determine the prevalence of osteoporosis in subgroups of COPD patients. * To look for risk factors of osteoporosis in COPD patients. * To create sub-groups for prospective research concerning the effects of bisphosphonates on osteoporosis variables in COPD patients. Study Design: Patients diagnosed with COPD (according to the American Thoracic Society \[ATS\] guidelines and divided in stages according to the Global Initiative on Obstructive Lung Diseases \[GOLD\]-classification) who visit the out-patient clinic of pulmonology of the Catharina Hospital Eindhoven will be asked to participate in the trial. A database will be created (prospectively) of the (medical) information about these patients, which will be analysed retrospective. To gather information we will use the medical records, a questionnaire, a blood sample, long function testing including a 6-minute walking test and a DEXA-scan.

Interventions

None listed

Sponsors

Catharina Ziekenhuis Eindhoven
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * Men and women * COPD according to the ATS-guidelines, divided in severity according to the GOLD criteria * Written consent

Exclusion criteria

* Age \< 18 years * No written consent

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026