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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01318174
Other study ID # LE-KE
Secondary ID
Status Completed
Phase N/A
First received March 17, 2011
Last updated July 7, 2014
Start date April 2011
Est. completion date April 2013

Study information

Verified date July 2014
Source Sykehuset Innlandet HF
Contact n/a
Is FDA regulated No
Health authority Norway: Regional Ethics Commitee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the prevalence of pulmonary embolism in our population of Chronic Obstructive Pulmonary Disease (COPD) patients admitted to hospital with dyspnea. The patients will undergo investigation for pulmonary embolism, according to current guidelines.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date April 2013
Est. primary completion date April 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- known or suspected COPD

- COPD-exacerbation

Exclusion Criteria:

- other causes of dyspnea

- unable to perform CT pulmonary angio (contrast allergy, pregnancy)

- already included in the study (each patient included only once)

- use of anticoagulants

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Norway Sykehuset Innlandet Lillehammer Oppland

Sponsors (1)

Lead Sponsor Collaborator
Sykehuset Innlandet HF

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of pulmonary embolism in exacerbations of COPD one year No
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