Osteoporosis and Chronic Obstructive Pulmonary Disease (COPD)
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Purpose
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.
| Condition |
|---|
|
COPD Osteoporosis Osteopenia |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Cross-Sectional |
| Official Title: | Osteoporosis and COPD (Making of a Database) |
| Estimated Enrollment: | 250 |
| Study Start Date: | April 2005 |
| Study Completion Date: | January 2009 |
| Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Chronic Obstructive Pulmonary Disease Patients visiting the pulmonary outpatient clinic of the Catharina Hospital Eindhoven.
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
Contacts and Locations| Netherlands | |
| Catharina Hospital Eindhoven | |
| Eindhoven, Noord-Brabant, Netherlands, 5602 ZA | |
| Principal Investigator: | Lidwien Graat, MD | Catharina Hospital Eindhoven (Department of Pulmonology) |
More Information
No publications provided
| Responsible Party: | Lidwien Graat-Verboom/MD (principal investigator), Catharina Hospital Eindhoven |
| ClinicalTrials.gov Identifier: | NCT00231127 History of Changes |
| Other Study ID Numbers: | M05-1522 |
| Study First Received: | October 3, 2005 |
| Last Updated: | November 9, 2009 |
| Health Authority: | Netherlands: Medical Ethics Review Committee (METC) |
Keywords provided by Catharina Ziekenhuis Eindhoven:
|
COPD Osteoporosis Osteopenia |
Glucocorticoids GOLD BODE |
Additional relevant MeSH terms:
|
Lung Diseases Pulmonary Disease, Chronic Obstructive Bone Diseases, Metabolic Osteoporosis |
Lung Diseases, Obstructive Respiratory Tract Diseases Bone Diseases Musculoskeletal Diseases |
ClinicalTrials.gov processed this record on May 19, 2013