Clinical Trials Directory

Trials / Unknown

UnknownNCT01626521

Value of Prothrombin Fragment F1+2 in the Diagnosis of Pulmonary Embolism in Patients With Chronic Obstructive Pulmonary Disease (COPD) Exacerbation

Status
Unknown
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
Hillel Yaffe Medical Center · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To access the clinical usefulness of F1+2 in the diagnosis of PE in patients with AECOPD who require hospitalization. Specifically, to determine whether F1+2 may have an additional value in the subgroup of patients with an abnormal D-dimer,to determine whether it may increase the proportion of patients in whom PE can be safely ruled out and to determine the sensitivity, specificity and NPV of F1+2 at various cut-off values.

Conditions

Interventions

TypeNameDescription
OTHERCT pulmonary angio, blood testsCT pulmonary angiography to determine PE and laboratory blood tests to determine prothrombin fragments F1+2 in blood of COPD patients

Timeline

Start date
2012-07-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2012-06-22
Last updated
2012-06-22

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01626521. Inclusion in this directory is not an endorsement.

Value of Prothrombin Fragment F1+2 in the Diagnosis of Pulmonary Embolism in Patients With Chronic Obstructive Pulmonary (NCT01626521) · Clinical Trials Directory