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Clinical Trials/NCT00231127
NCT00231127
Completed
Not Applicable

Osteoporosis and COPD (Making of a Database)

Catharina Ziekenhuis Eindhoven1 site in 1 country250 target enrollmentApril 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD
Sponsor
Catharina Ziekenhuis Eindhoven
Enrollment
250
Locations
1
Status
Completed
Last Updated
16 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 2005
End Date
January 2009
Last Updated
16 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Catharina Ziekenhuis Eindhoven

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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