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Osteoporosis and Chronic Obstructive Pulmonary Disease (COPD)

Catharina Hospital logo

Catharina Hospital

Status

Completed

Conditions

Osteopenia
Osteoporosis
COPD

Study type

Observational

Funder types

Other

Identifiers

NCT00231127
M05-1522

Details and patient eligibility

About

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.

Full 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.

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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