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Clinical Trials/NCT00614900
NCT00614900
Completed
Not Applicable

Prevalence and Influence of Pulmonary Hypertension in COPD Patients

University of Aarhus1 site in 1 country117 target enrollmentMarch 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD
Sponsor
University of Aarhus
Enrollment
117
Locations
1
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The prevalence of an increased pulmonary blood pressure amongst patients with chronic obstructive pulmonary disease (COPD)is unclear. So is the impact of abnormal pulmonary blood pressure on symptoms. The aim of this study is to determine the prevalence of an increased pulmonary blood pressure in 200 patients with COPD. Furthermore we will investigate if lung function test results and blood tests can predict an increased pulmonary blood pressure, and explore whether COPD patients with a high pulmonary blood pressure have more symptoms that their co-patients.

Detailed Description

The prevalence of pulmonary hypertension in patients with chronic obstructive pulmonary disease (COPD) is unclear. The presence of an abnormally increased pulmonary blood pressure worsens the prognosis of COPD, but the patients are not currently diagnosed or treated for pulmonary hypertension. The aim of this study is to determine the prevalence of pulmonary hypertension in 200 patients with COPD and explore whether it worsens functional capacity and symptoms. Furthermore we will look into whether blood gas values, NT-proBNP, CRP and lung function test result can predict which patients are at risk of having pulmonary hypertension. Methods: All patients will be screened by echocardiography. Those with signs of pulmonary hypertension will be admitted to right heart catheterization for direct measurements of pulmonary haemodynamics. All patients will perform a 6 minutes walk test and spirometry. Blood levels of NT-proBNP and CRP will be measured. Life quality by the St. George Questionnaire and contacts to the health care system is also assessed. Differences in these parameters are analyzed among patients with no, moderate or severe pulmonary hypertension.

Registry
clinicaltrials.gov
Start Date
March 2008
End Date
March 2011
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Charlotte Andersen

MD

University of Aarhus

Eligibility Criteria

Inclusion Criteria

  • Diagnosis of COPD
  • Prior admittance to hospital with exacerbation in COPD
  • Informed consent

Exclusion Criteria

  • Exacerbation in COPD less than 6 weeks before examination

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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