Diagnosis Exclusion of Recurrent Deep Vein Thrombosis of the Lower Limbs (ULTREC)
Primary Purpose
Deep Vein Thrombosis
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Colour doppler ultrasound with or without D-dimer test
Sponsored by
About this trial
This is an interventional diagnostic trial for Deep Vein Thrombosis focused on measuring Deep vein thrombosis, Recurrence, Diagnostic strategy, Colour doppler ultrasound, D-dimer
Eligibility Criteria
Inclusion Criteria:
- Age >= 18 years
- Known history of objectively documented deep vein thrombosis of the lower limb (with or without pulmonary embolism)
- Out-patients referred for clinically suspected acute recurrent ipsilateral DVT of the lower limb i.e. the occurrence of new symptoms and signs of DVT or the increase of symptoms and signs in patients with post-thrombotic syndrome
- Patients covered by social security or equivalent regimen
- Signed and dated informed consent
Exclusion Criteria:
- Known current pregnancy
- Any condition, which, in the opinion of the investigator may prevent him from performing the colour doppler ultrasound test (plaster cast, inaccessible vein segment after abdominal or pelvic surgery, or other causes that may lead to a technically inadequate CDUS)
- Delay from onset of symptoms to inclusion of more than 10 days
- Therapeutic anticoagulation for more than 48 hours in the two days prior to consent or a need for long term anticoagulation
- Prophylactic anticoagulation for more than 48 hours in the two days prior to consent
- Clinical symptoms of pulmonary embolism
- Life expectancy less than 3 months
- Patient unable to adhere to protocol or follow-up visits and contacts
- Participants under legal guardianship or incapacitation
- Patient already enrolled in a deep vein thrombosis (DVT) diagnostic research
Sites / Locations
- Centre Hospitalier de Vichy
- Centre Hospitalier Universitaire de Nice
- Centre Hospitalier de Carcassonne
- Centre d'angiologie
- APHM La Timone
- Cabinet libéral Pung
- Cabinet libéral Dias
- Cabinet libéral Sidoli
- Cabinet libéral El Haddad
- Cabinet libéral De Mari
- Cabinet libéral Secondi
- Centre Hospitalier Universitaire Bocage
- Centre Hospitalier Universitaire François Mitterrand
- Centre hospitalier Universitaire Cavale Blanche
- Centre Hospitalier Universitaire de Nîmes
- Centre Hospitalier d'Auch
- Cabinet libéral Cazaux
- Hôpital Saint André
- Centre de medicine vasculaire interventionnel
- Cabinet libéral Casanova
- Cabinet libéral Bonavita
- Cabinet libéral Bourrinet
- Centre Hospitalier Universitaire Rangueil
- Clinique Rive Gauche
- Cabinet libéral Wagner
- Cabinet libéral Esteve
- Centre Hospitalier Universitaire de Montpellier
- Centre d'explorations vasculaires
- Centre Hospitalier Universitaire de Rennes
- Centre Hospitalier Universitaire de Grenoble
- Centre Hospitalier Universitaire Nord
- Centre Hospitalier Universitaire d'Angers
- Centre Hospitalier Universitaire de Nancy
- Espace Artois Santé
- Centre Hospitalier Universitaire de Clermont-Ferrand
- Hôpital Edouard Herriot
- Centre Hospitalier Universitaire d'Amiens
- Cabinet libéral Besancon - polyclinique des Fleurs
- Clinique des Fleurs
- Cabinet libéral Richard
- Cabinet libéral Ben Sedrine
- Cabinet libéral Riviere
- Cabinet libéral Zimmermann
- Centre Hospitalier Intercommunal Toulon La Seyne sur Mer
- Hôpital Saint Joseph
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Diagnostic strategy
Arm Description
Colour doppler ultrasound (CDUS) with or without D-dimer test to rule-in or rule-out deep vein thrombosis recurrence
Outcomes
Primary Outcome Measures
Adjudicated symptomatic venous thromboembolic events
Rate of adjudicated symptomatic venous thromboembolic (VTE) events among patients not treated by anticoagulants according to the diagnostic strategy
The criteria for recurrent VTE include:
objectively confirmed pulmonary embolism (PE) by either CT pulmonary angiography or ventilation-perfusion scan,
death due to PE,
and recurrent DVT of the leg Death, cause of death, VTE comprising isolated proximal or distal DVT and PE (with or without DVT), will be adjudicated by an independent clinical event committee blinded to the classification of the diagnostic strategy.
Secondary Outcome Measures
Prevalence of deep vein thrombosis recurrence
Proportion of patients with a new DVT among all patients included based on the results of the diagnostic tests used in the strategy and on the occurrence of VTE events during follow-up in patients untreated
Proportion of patients tested negative
Proportion of patients tested negative by the strategy for DVT recurrence among all patients included
Proportion of complete patients
Proportion of patients who completed the strategy
Bleeding complication occurrence
The occurrence of bleeding complications will be assessed among all patients included during a 3-month follow-up period. The severity of these complications will be adjudicated by the independent clinical event committee according to the International Society on Thrombosis and Haemostasis classification criteria.
Correlation of possible strategy failure in not anticoagulated patients and patient characteristics
Identification of clinical and ultrasound factors which could explain failure of the strategy in non anticoagulated patients
Prevalence of isolated superficial vein thrombosis
Proportion of patients with isolated superficial vein thrombosis during a 3-month follow-up among all patients included
Full Information
NCT ID
NCT03868956
First Posted
March 8, 2019
Last Updated
October 23, 2023
Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Collaborators
Centre Hospitalier Universitaire de Saint Etienne, Investigation network on venous thrombo-embolism
1. Study Identification
Unique Protocol Identification Number
NCT03868956
Brief Title
Diagnosis Exclusion of Recurrent Deep Vein Thrombosis of the Lower Limbs
Acronym
ULTREC
Official Title
Safety of a Management Strategy Based on Colour Doppler ULTrasound and D-Dimer Testing for the Diagnosis Exclusion of RECurrent Deep Vein Thrombosis of the Lower Limbs. The ULTREC Project
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
January 17, 2020 (Actual)
Primary Completion Date
January 30, 2023 (Actual)
Study Completion Date
January 30, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer
Collaborators
Centre Hospitalier Universitaire de Saint Etienne, Investigation network on venous thrombo-embolism
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose is to assess the safety of a management strategy based on colour doppler ultrasound (CDUS) and D-Dimer test results for the diagnosis exclusion of recurrent deep vein thrombosis (DVT) of the lower limbs.
DVT recurrence requires using anticoagulant treatment to prevent thrombosis progression. Given an increased bleeding risk with prolonged treatment, an accurate diagnosis for recurrence is needed. However, the diagnosis of a new thrombosis in a previously involved leg is difficult. Imaging modalities and criteria that are currently used for the diagnosis may be equivocal and unable to discriminate between an old clot and a new one recently developed at the same site. An increase in vein diameter after vein compression by the ultrasound probe was suggested as a diagnostic criterion for a new DVT. This method has many limitations in clinical practice, mainly a lack of availability of a previous measurement and a poor inter-observer agreement.
Colour Doppler ultrasound enables to study both the thrombus and the blood flow characteristics that might help to overcome these limitations. CDUS is a well-known method for the diagnosis of vascular diseases and is used in every day clinical practice for the diagnosis of a first DVT and DVT recurrence but CDUS has never been assessed for DVT recurrence in a study. The diagnosis of DVT recurrence may be easily established using the same criteria as for a first DVT episode. Our hypothesis is that CDUS associated with D-Dimer can safely rule out the diagnosis of DVT recurrence while maintaining a good specificity.
The strategy consists in performing first a CDUS that helps to classify patients as having (positive CDUS) or not having (negative CDUS) a new thrombosis. In the case of an equivocal CDUS, a D-Dimer test is performed. If the D-dimer is normal, the diagnosis of DVT recurrence is ruled out and the patient is not treated. If the D-dimer is abnormal, the diagnosis cannot be excluded nor confirmed and a second CDUS is performed on D7±2. Meanwhile, patients are not treated by anticoagulants. An unchanged CDUS on D7±2 qualifies patients as free from a new DVT and they are not treated. Conversely a change in CDUS qualifies patients as having a new DVT which requires anticoagulant treatment.
All patients have a 3-month follow-up for the assessment of potential venous thromboembolic events.
Detailed Description
Venous thromboembolism (VTE) recurrence is a common situation after stopping anticoagulant treatment. This recurrence requires extended anticoagulant therapy to prevent thrombosis progression and embolization, but given an increased bleeding risk with prolonged treatment, an accurate diagnosis for VTE recurrence is needed.
Unfortunately, there is no reference standard for the diagnosis of deep vein thrombosis (DVT) recurrence and objective and accurate diagnostic methods are lacking. Clinical assessment does not allow discriminating between a previous and a recent thrombosis and there is no clinical prediction rule specific to the suspicion of DVT recurrence. D-dimer assays alone may not be able to safely exclude the diagnosis of DVT recurrence, and they have not been sufficiently validated in combination with clinical probability. The same holds for imaging modalities because normalisation rate after proximal DVT is low and a "residual thrombosis" may make difficult the diagnosis of a new thrombosis episode at the same site. Phlebography is non-diagnostic in 33% of cases. CT-venography has never been evaluated and MRI direct thrombus imaging (MRDTI) although very promising is still under evaluation.
As compression ultrasound (CUS) may be equivocal due to a residual thrombosis, a comparison to baseline measurements of residual vein diameter after full compression at the common femoral and the popliteal vein segments in cross-sectional plane has been suggested with an increase in diameter superior to 2 or 4 mm as a diagnosis criterion. This method has many major limitations related to: 1/the need for a previous measurement almost never available in practice, 2/ the potential for recurrence at a different site than that previously measured, 3/ a poor inter-observer agreement or at least inconsistent inter-observer variability between studies, 4/ small sample sizes in diagnostic accuracy and in diagnostic management studies and 5/ lack of external validation. Due to these limitations, recurrent ipsilateral DVT is mainly diagnosed by CUS when it occurs in a new or a normalised vein segment.
Colour Doppler ultrasound (CDUS) enables to study both the thrombus and the blood flow characteristics that might help to overcome the limitations of CUS and diameter measurements. Although CDUS has never been assessed for DVT recurrence in a study, it is used in every day clinical practice and seems very helpful. The diagnosis may be easily established using the same CDUS criteria as for a first DVT episode. Our hypothesis is that CDUS associated with D-Dimer can safely exclude the diagnosis of recurrent DVT while maintaining a good specificity.
The strategy consists in performing first a CDUS that helps to classify patients as having (positive CDUS) or not having (negative CDUS) a new thrombosis. In the case of an equivocal (non-diagnostic) CDUS, a D-Dimer test is performed followed by repeat CDUS on D7±2 if D-dimer test result is abnormal. Meanwhile, patients are not treated by anticoagulants. A negative D-dimer test or an unchanged CDUS on D7±2 qualifies patients as free from a new DVT. Conversely a change in CDUS qualifies patients as having a new DVT. Only patients with a new DVT are treated. All patients have a 3-month follow-up for the assessment of venous thromboembolic and bleeding events by an independent adjudication committee.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Deep Vein Thrombosis
Keywords
Deep vein thrombosis, Recurrence, Diagnostic strategy, Colour doppler ultrasound, D-dimer
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
466 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Diagnostic strategy
Arm Type
Experimental
Arm Description
Colour doppler ultrasound (CDUS) with or without D-dimer test to rule-in or rule-out deep vein thrombosis recurrence
Intervention Type
Diagnostic Test
Intervention Name(s)
Colour doppler ultrasound with or without D-dimer test
Intervention Description
Positive CDUS: anticoagulant treatment
Negative CDUS: no anticoagulant treatment
Non diagnostic CDUS : reference to routine D-dimer test
Negative test : no anticoagulant treatment
Positive test : second CDUS 7 days (±2) after first one
No change in CDUS : no anticoagulant treatment
Change in CDUS : anticoagulant treatment
Primary Outcome Measure Information:
Title
Adjudicated symptomatic venous thromboembolic events
Description
Rate of adjudicated symptomatic venous thromboembolic (VTE) events among patients not treated by anticoagulants according to the diagnostic strategy
The criteria for recurrent VTE include:
objectively confirmed pulmonary embolism (PE) by either CT pulmonary angiography or ventilation-perfusion scan,
death due to PE,
and recurrent DVT of the leg Death, cause of death, VTE comprising isolated proximal or distal DVT and PE (with or without DVT), will be adjudicated by an independent clinical event committee blinded to the classification of the diagnostic strategy.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Prevalence of deep vein thrombosis recurrence
Description
Proportion of patients with a new DVT among all patients included based on the results of the diagnostic tests used in the strategy and on the occurrence of VTE events during follow-up in patients untreated
Time Frame
Up to 3 months
Title
Proportion of patients tested negative
Description
Proportion of patients tested negative by the strategy for DVT recurrence among all patients included
Time Frame
A day if the diagnostic strategy is conclusive (either positive or negative) at day 0, or 7 days if it is inconclusive
Title
Proportion of complete patients
Description
Proportion of patients who completed the strategy
Time Frame
3 months
Title
Bleeding complication occurrence
Description
The occurrence of bleeding complications will be assessed among all patients included during a 3-month follow-up period. The severity of these complications will be adjudicated by the independent clinical event committee according to the International Society on Thrombosis and Haemostasis classification criteria.
Time Frame
3 months
Title
Correlation of possible strategy failure in not anticoagulated patients and patient characteristics
Description
Identification of clinical and ultrasound factors which could explain failure of the strategy in non anticoagulated patients
Time Frame
3 months
Title
Prevalence of isolated superficial vein thrombosis
Description
Proportion of patients with isolated superficial vein thrombosis during a 3-month follow-up among all patients included
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >= 18 years
Known history of objectively documented deep vein thrombosis of the lower limb (with or without pulmonary embolism)
Out-patients referred for clinically suspected acute recurrent ipsilateral DVT of the lower limb i.e. the occurrence of new symptoms and signs of DVT or the increase of symptoms and signs in patients with post-thrombotic syndrome
Patients covered by social security or equivalent regimen
Signed and dated informed consent
Exclusion Criteria:
Known current pregnancy
Any condition, which, in the opinion of the investigator may prevent him from performing the colour doppler ultrasound test (plaster cast, inaccessible vein segment after abdominal or pelvic surgery, or other causes that may lead to a technically inadequate CDUS)
Delay from onset of symptoms to inclusion of more than 10 days
Therapeutic anticoagulation for more than 48 hours in the two days prior to consent or a need for long term anticoagulation
Prophylactic anticoagulation for more than 48 hours in the two days prior to consent
Clinical symptoms of pulmonary embolism
Life expectancy less than 3 months
Patient unable to adhere to protocol or follow-up visits and contacts
Participants under legal guardianship or incapacitation
Patient already enrolled in a deep vein thrombosis (DVT) diagnostic research
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoine Elias, MD
Organizational Affiliation
Centre Hospitalier Intercommunal Toulon La Seyne sur Mer
Official's Role
Study Director
Facility Information:
Facility Name
Centre Hospitalier de Vichy
City
Vichy
State/Province
Allier
ZIP/Postal Code
03200
Country
France
Facility Name
Centre Hospitalier Universitaire de Nice
City
Nice
State/Province
Alpes-Maritimes
ZIP/Postal Code
06001
Country
France
Facility Name
Centre Hospitalier de Carcassonne
City
Carcassonne
State/Province
Aude
ZIP/Postal Code
1060
Country
France
Facility Name
Centre d'angiologie
City
Carcassonne
State/Province
Aude
ZIP/Postal Code
11000
Country
France
Facility Name
APHM La Timone
City
Marseille
State/Province
Bouches Du Rhône
ZIP/Postal Code
13385
Country
France
Facility Name
Cabinet libéral Pung
City
Aubagne
State/Province
Bouches-du-Rhône
ZIP/Postal Code
13400
Country
France
Facility Name
Cabinet libéral Dias
City
Istres
State/Province
Bouches-du-Rhône
ZIP/Postal Code
13800
Country
France
Facility Name
Cabinet libéral Sidoli
City
Marseille
State/Province
Bouches-du-Rhône
ZIP/Postal Code
13003
Country
France
Facility Name
Cabinet libéral El Haddad
City
Marseille
State/Province
Bouches-du-Rhône
ZIP/Postal Code
13011
Country
France
Facility Name
Cabinet libéral De Mari
City
Ajaccio
State/Province
Corse Du Sud
ZIP/Postal Code
20090
Country
France
Facility Name
Cabinet libéral Secondi
City
Ajaccio
State/Province
Corse Du Sud
ZIP/Postal Code
20090
Country
France
Facility Name
Centre Hospitalier Universitaire Bocage
City
Dijon
State/Province
Cote d'Or
ZIP/Postal Code
21079
Country
France
Facility Name
Centre Hospitalier Universitaire François Mitterrand
City
Dijon
State/Province
Côte d'Or
ZIP/Postal Code
21079
Country
France
Facility Name
Centre hospitalier Universitaire Cavale Blanche
City
Brest
State/Province
Finistère
ZIP/Postal Code
29609
Country
France
Facility Name
Centre Hospitalier Universitaire de Nîmes
City
Nîmes
State/Province
Gard
ZIP/Postal Code
30029
Country
France
Facility Name
Centre Hospitalier d'Auch
City
Auch
State/Province
Gers
ZIP/Postal Code
32000
Country
France
Facility Name
Cabinet libéral Cazaux
City
Auch
State/Province
Gers
Country
France
Facility Name
Hôpital Saint André
City
Bordeaux
State/Province
Gironde
ZIP/Postal Code
33075
Country
France
Facility Name
Centre de medicine vasculaire interventionnel
City
Langon
State/Province
Gironde
ZIP/Postal Code
33210
Country
France
Facility Name
Cabinet libéral Casanova
City
Bastia
State/Province
Haute Corse
ZIP/Postal Code
20600
Country
France
Facility Name
Cabinet libéral Bonavita
City
Bastia
State/Province
Haute-Corse
ZIP/Postal Code
20200
Country
France
Facility Name
Cabinet libéral Bourrinet
City
Balma
State/Province
Haute-Garonne
ZIP/Postal Code
31130
Country
France
Facility Name
Centre Hospitalier Universitaire Rangueil
City
Toulouse
State/Province
Haute-Garonne
ZIP/Postal Code
31059
Country
France
Facility Name
Clinique Rive Gauche
City
Toulouse
State/Province
Haute-Garonne
ZIP/Postal Code
31076
Country
France
Facility Name
Cabinet libéral Wagner
City
Lourdes
State/Province
Hautes-Pyrénées
ZIP/Postal Code
65100
Country
France
Facility Name
Cabinet libéral Esteve
City
Tarbes
State/Province
Hautes-Pyrénées
ZIP/Postal Code
65000
Country
France
Facility Name
Centre Hospitalier Universitaire de Montpellier
City
Montpellier
State/Province
Hérault
ZIP/Postal Code
34295
Country
France
Facility Name
Centre d'explorations vasculaires
City
Paris
State/Province
Ile-de-France
ZIP/Postal Code
75116
Country
France
Facility Name
Centre Hospitalier Universitaire de Rennes
City
Rennes
State/Province
Ille-et-Vilaine
ZIP/Postal Code
35033
Country
France
Facility Name
Centre Hospitalier Universitaire de Grenoble
City
Grenoble
State/Province
Isère
ZIP/Postal Code
38700
Country
France
Facility Name
Centre Hospitalier Universitaire Nord
City
Saint-Étienne
State/Province
Loire
ZIP/Postal Code
42055
Country
France
Facility Name
Centre Hospitalier Universitaire d'Angers
City
Angers
State/Province
Maine-et-Loire
ZIP/Postal Code
49933
Country
France
Facility Name
Centre Hospitalier Universitaire de Nancy
City
Nancy
State/Province
Meurthe Et Moselle
ZIP/Postal Code
54511
Country
France
Facility Name
Espace Artois Santé
City
Arras
State/Province
Pas-de-Calais
ZIP/Postal Code
62000
Country
France
Facility Name
Centre Hospitalier Universitaire de Clermont-Ferrand
City
Clermont-Ferrand
State/Province
Puy-de-Dôme
ZIP/Postal Code
63000
Country
France
Facility Name
Hôpital Edouard Herriot
City
Lyon
State/Province
Rhône
ZIP/Postal Code
69003
Country
France
Facility Name
Centre Hospitalier Universitaire d'Amiens
City
Amiens
State/Province
Somme
ZIP/Postal Code
80054
Country
France
Facility Name
Cabinet libéral Besancon - polyclinique des Fleurs
City
Ollioules
State/Province
Var
ZIP/Postal Code
83190
Country
France
Facility Name
Clinique des Fleurs
City
Ollioules
State/Province
Var
ZIP/Postal Code
83190
Country
France
Facility Name
Cabinet libéral Richard
City
Sanary-sur-Mer
State/Province
Var
ZIP/Postal Code
83110
Country
France
Facility Name
Cabinet libéral Ben Sedrine
City
Six-Fours-les-Plages
State/Province
Var
ZIP/Postal Code
83140
Country
France
Facility Name
Cabinet libéral Riviere
City
Six-Fours-les-Plages
State/Province
Var
ZIP/Postal Code
83140
Country
France
Facility Name
Cabinet libéral Zimmermann
City
Six-Fours-les-Plages
State/Province
Var
ZIP/Postal Code
83140
Country
France
Facility Name
Centre Hospitalier Intercommunal Toulon La Seyne sur Mer
City
Toulon
State/Province
Var
ZIP/Postal Code
83056
Country
France
Facility Name
Hôpital Saint Joseph
City
Paris
ZIP/Postal Code
75674
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
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Diagnosis Exclusion of Recurrent Deep Vein Thrombosis of the Lower Limbs
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