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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01078792
Other study ID # 0001-10
Secondary ID
Status Not yet recruiting
Phase N/A
First received March 1, 2010
Last updated March 1, 2010

Study information

Verified date March 2010
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

To determine the possible association of prothrombin fragments 1+2 elevation with incidents of pulmonary embolism in patients with COPD exacerbation.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- COPD exacerbation

- Able to give informed consent

- Able to perform spirometry

Exclusion Criteria:

- Known malignancy

- Known hypercoagulable state

- Receiving anticoagulant treatment

- Pregnancy

- Renal failure

- Allergy to Iodine

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
CT pulmonary angio, blood tests


Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

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