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

NCT ID: NCT00860106

Last Updated: 2011-10-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

222 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-03-31

Study Completion Date

2011-05-31

Brief Summary

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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.

Detailed Description

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

Conditions

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Previous Vka Treatment Previous Proximal VTE

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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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.

Group Type OTHER

ED, DDimers and phone follow up

Intervention Type OTHER

ED score, DDimers level and phone questionnary

Interventions

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ED, DDimers and phone follow up

ED score, DDimers level and phone questionnary

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Gilles PERNOD, Professor

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Grenoble

Locations

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University Hospital

Amiens, , France

Site Status

Cabinet Medical

Annecy, , France

Site Status

HOSPITAL

Annecy, , France

Site Status

Cabinet Medical

Bourgoin, , France

Site Status

Cabinet Medical

Chalon-sur-Saône, , France

Site Status

HOSPITAL

Chambéry, , France

Site Status

Cabinet Medical

Crolles, , France

Site Status

Cabinet Medical

Fontaine, , France

Site Status

Vascular Medecine Departement - University Hospital of Grenoble

Grenoble, , France

Site Status

Cabinet Medical

Grenoble, , France

Site Status

Clinique Mutualiste les eaux claires

Grenoble, , France

Site Status

Cabinet Medical

Meylan, , France

Site Status

Cabinet Medical

Pontcharra, , France

Site Status

Cabinet Medical

Saint-Égrève, , France

Site Status

CMC Les Petites Roches

Saint-Hilaire, , France

Site Status

Cabinet Medical

Voiron, , France

Site Status

Countries

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France

References

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PMID: 11848459 (View on PubMed)

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Piovella F, Crippa L, Barone M, Vigano D'Angelo S, Serafini S, Galli L, Beltrametti C, D'Angelo A. Normalization rates of compression ultrasonography in patients with a first episode of deep vein thrombosis of the lower limbs: association with recurrence and new thrombosis. Haematologica. 2002 May;87(5):515-22.

Reference Type BACKGROUND
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Prandoni P, Lensing AW, Prins MH, Bernardi E, Marchiori A, Bagatella P, Frulla M, Mosena L, Tormene D, Piccioli A, Simioni P, Girolami A. Residual venous thrombosis as a predictive factor of recurrent venous thromboembolism. Ann Intern Med. 2002 Dec 17;137(12):955-60. doi: 10.7326/0003-4819-137-12-200212170-00008.

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Reference Type BACKGROUND
PMID: 12965989 (View on PubMed)

Other Identifiers

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DCIC 04 22

Identifier Type: -

Identifier Source: org_study_id