Echo Doppler (ED )Score and D-dimer (DD) Level in the Evaluation of VTE Recurrence After Anticoagulant Treatment Cessation (VAPRED)

October 10, 2011 updated by: University Hospital, Grenoble

Study of Predictive Echo Doppler Score and D-dimer Level in Evaluation of the Thromboembolic Event Recurrence After Anticoagulant Treatment Cessation.

The purpose of this trial is to perform a prospective multicentric study to determine predictive ED score and D-dimer level in the evaluation of the thromboembolic event recurrence after anticoagulant treatment cessation.

The patients are included in the study from the anticoagulant treatment cessation. An ED score and a blood sample are performed at this time and one month later. Then, the patients are followed up by phone for 2 years.

Study Overview

Detailed Description

DDimer levels are centralized in University Hospital of Grenoble at the end of the study

Study Type

Interventional

Enrollment (Actual)

222

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Amiens, France
        • University Hospital
      • Annecy, France
        • Cabinet Médical
      • Annecy, France
        • Hospital
      • Bourgoin Jallieu, France
        • Cabinet Médical
      • Chalon Sur Saone, France
        • Cabinet Médical
      • Chambery, France
        • Hospital
      • Crolles, France
        • Cabinet Médical
      • Fontaine, France
        • Cabinet Médical
      • Grenoble, France, 38043
        • Vascular Medecine Departement - University Hospital of Grenoble
      • Grenoble, France
        • Cabinet Médical
      • Grenoble, France
        • Clinique Mutualiste les eaux claires
      • Meylan, France
        • Cabinet Médical
      • Pontcharra, France
        • Cabinet Médical
      • Saint Egreve, France
        • Cabinet Médical
      • Saint Hilaire Du Touvet, France
        • Cmc Les Petites Roches
      • Voiron, France
        • Cabinet Médical

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • > 18 and <80 years old
  • First or second treated proximal VTE event (+/- Pulmonary embolism)
  • Signed informed consent

Exclusion Criteria:

  • Active cancer or currently treated
  • Previous VTE>2
  • Long term anticoagulant treatment for VTE diseases
  • Long term anticoagulant treatment for other diseases
  • Pregnancy, parturient or breast feeding
  • Person deprived of freedom by judicial or administrative decision
  • Consent unsigned

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Non-Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Follow up

ED score and DDimer level of patients who have stopped their VKA treatment (after the first or the second previous proximal VTE).

Phone follow up for 2 years.

ED score, DDimers level and phone questionnary

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
VTE event recurrence
Time Frame: 0-2 years
0-2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gilles PERNOD, Professor, University Hospital, Grenoble

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2005

Primary Completion (Actual)

May 1, 2010

Study Completion (Actual)

May 1, 2011

Study Registration Dates

First Submitted

March 10, 2009

First Submitted That Met QC Criteria

March 10, 2009

First Posted (Estimate)

March 11, 2009

Study Record Updates

Last Update Posted (Estimate)

October 12, 2011

Last Update Submitted That Met QC Criteria

October 10, 2011

Last Verified

October 1, 2011

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DCIC 04 22

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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