This trial is active, not recruiting.

Conditions deep venous thrombosis, pulmonary embolism, d-dimer
Phase phase 4
Sponsor Diagnostica Stago
Collaborator University Hospital, Grenoble
Start date November 2011
End date November 2016
Trial size 2426 participants
Trial identifier NCT01221805, DCIC 10 18


The purpose of this study is to demonstrate the ability of STA® Liatest® D-Di combined with a clinical pretest probability (PTP) to safely exclude pulmonary embolism (PE) or Deep Venous Thrombosis (DVT) in a 3 month follow-up.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective

Primary Outcomes

To demonstrate the ability of STA Liatest DDi combined with a clinical pretest probability (PTP) to safely exclude pulmonary embolism or deep venous thrombosis in a 3 month follow-up
time frame: at 3 months

Secondary Outcomes

1. To analyse results homogeneity (inter-centers) in the group "positive D-dimer result and negative diagnosis" (descriptive statistics only). 2. To determine prevalence of VTE in PTP high patients based on imaging results
time frame: at 3 months

Eligibility Criteria

Male or female participants up to 80 years old.

INCLUSION CRITERIA 1. Patient is < 80 years old. 2. Patient presenting at least one of these symptoms indicative of proximal DVT or PE: - symptoms for proximal DVT: leg pain, tenderness (discomfort through palpation), leg swelling, and /or edema, - symptoms for PE: hemoptysis, lung related chest pain, dyspnea. 3. Patient provides written informed consent to participate in the study (or verbal no-opposition, as allowed by local regulations) 4. Patient is willing to comply with specified follow-up evaluation at 3 months and can be contacted by telephone EXCLUSION CRITERIA 1. Patient presenting with a condition that may be associated with increased D-dimer levels, even in the absence of VTE, such as: - Fibrinolytic therapy within the previous seven (7) days, - Bone fracture or surgery (with general anesthesia longer than thirty (30) minutes) within the previous one (1) month, - Deep hematoma diagnosed by imaging techniques within the previous one (1) month, - Disseminated malignancies and active cancer (active cancer defined as: cancer for which therapeutic or palliative treatment is either ongoing at the time of enrolment or has stopped less than six (6) months before enrolment), - Sepsis, severe infections, pneumonia within the previous 1 month, - Known liver cirrhosis, - Pregnancy or post-partum within the previous 1 month, - Atherosclerotic vascular disease thrombosis within the previous 1month (e.g. myocardial infarction, stroke, coronary syndrome, peripheral artery disease stage III or IV), - Sickle cell disease, 2. Patients presenting with a suspect thrombotic event related to catheter implantation 3. Ongoing therapeutic anticoagulants (curative and preventive treatment) starting twenty four (24) hours or more before the D-dimer is measured 4. Previous anticoagulant therapy stopped less than three (3) months before the D-dimer is measured 5. Patients with previous DVT/PE occurred less than three (3) months from screening. 6. Suspect thrombotic events in other locations at screening, including distal to the knee and upper extremity DVT (based on standard of care examinations) 7. Patients with known tissue plasminogen activator (tPA) deficiency 8. Patient participating or who has participated within one month of enrollment in another investigational study 9. Major co-morbid condition(s) or other reasons that could limit the patient's ability to participate in the study or to comply with follow-up requirements, or impact the scientific integrity of the study

Additional Information

Official title STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Principal investigator GILLES PERNOD, MD PhD
Description The study population will be selected from prospective, consecutive ambulatory outpatients suspected of having venous thromboembolism. These patients will first be evaluated using the Wells score: - patients with low or moderate pretest probability will be considered for D-dimer testing, those with D-dimer positive will be considered for an imaging procedure, - patients with high pretest probability will be considered for an imaging procedure. Patients with "low or moderate" pretest probability and a negative D-Dimer result will be followed for 3 months to evaluate potential development of deep venous thrombosis and/or pulmonary embolism. These patients will be contacted by phone 3 month after their first visit.
Trial information was received from ClinicalTrials.gov and was last updated in January 2016.
Information provided to ClinicalTrials.gov by Diagnostica Stago.