Contribution of Lower Limb Venous Colour Doppler Ultrasound in the Diagnosis of Pulmonary Embolism Recurrence (RECHOPE)

Venous thromboembolic disease is a clinical entity including pulmonary embolism (PE) and deep vein thrombosis (DVT). It is a chronic disease with 30% recurrence rate at 10 years. In patients with recurrent PE clinical suspicion, an objective and accurate diagnostic method/strategy is warranted to exclude or confirm a PE new episode diagnosis and to decide on treatment initiation.

Recurrent PE diagnosis raises several issues related to the limitations of clinical scores, D-dimer testing, and diagnostic imaging used for a first episode diagnosis. Most importantly, residual obstruction on chest imaging reported in more than 50% of cases at 6 months can make it difficult to distinguish between an old and a new thrombosis in the absence of possible comparison with a previous imaging carried out under the same modalities.

There are currently few recommendations about the diagnostic strategy for patients with a recurrent PE clinical suspicion and these recommendations are not very consistent due to the lack of a validated strategy. None of current guidelines have included imaging-detectable lower-limb DVT within the strategies despite a reported high prevalence of PE-associated DVT. In one study using venography, 82% (95% CI 76.5 - 86.9) of angiographically-proven PE patients had an associated proximal or distal deep vein thrombosis, of which 42% were asymptomatic. In another study using lower-limb venous ultrasound, a proximal or distal DVT was detected in 93% (95% CI 85-97) of patients with PE.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In this study, patients with PE clinical suspicion and a previous PE episode have a standard diagnostic work-up based on clinical probability assessment, D-dimer testing and diagnostic imaging (pulmonary CT angiography, ventilation perfusion scan).

A bilateral lower-limb venous colour doppler ultrasound (CDUS) is performed in parallel in these patients as usually carried out in our hospital for the diagnosis management of patients with clinically suspected PE. This test is performed and interpreted by an independent sonographer unaware of the results of the standard diagnostic work-up.

Lower-limb venous CDUS is then compared to the results of the standard work-up as interpreted during expert panel meetings by members involved in the diagnosis and management of patients with PE and DVT.

Data will be collected both retrospectively and prospectively.

Study Type

Observational

Enrollment (Actual)

115

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

    • Var
      • Toulon, Var, France, 83056
        • CHITS

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult patients hospitalized for suspicion of pulmonary embolism recurrence

Description

Inclusion Criteria:

  • Adult consecutive patients (>= 18 years old)
  • Hospitalized for clinical suspicion of pulmonary embolism recurrence with at least one of the following symptoms: acute dyspnea or worsening of chronic dyspnea, chest pain, hemoptysis or syncope

Exclusion Criteria:

  • Time between onset of symptoms and diagnosis > 15 days
  • Pregnant women
  • Contra-indication to CT pulmonary angiography
  • Lower-limb CDUS not possible to perform for technical reasons
  • Lung scans not possible to perform for technical reasons

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

  • Observational Models: Cohort
  • Time Perspectives: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Adult patients hospitalized for suspicion of pulmonary embolism recurrence
Patients with at least one of the following symptoms: acute dyspnea or aggravation of chronic dyspnea, chest pain, hemoptysis or syncope
Comparison with conventional diagnosis strategy including a clinical probability score, D-dimers and chest imaging.
Other Names:
  • Diagnosis strategy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To evaluate lower-limb venous Color Doppler Ultrasound (CDUS) contribution to the conventional strategy used for pulmonary embolism recurrence diagnosis including a clinical probability score, D-dimers and chest imaging.
Time Frame: At diagnostic work-up (24 first hours following admission)

Proportion of patients for whom the lower-limb venous CDUS is positive. CDUS will be considered as positive if an acute DVT is shown with any of the following aspects:

  • Mobile thrombus
  • Completely occlusive thrombus
  • Sub-occlusive thrombus without deep venous reflux

Color Doppler Ultrasound will be considered as negative for a new thrombosis if the vein is compressible and there is no image of DVT, or if there are images of DVT sequelae only, with one of the following aspects:

  • Parietal residual sequelae
  • Partial obstruction with deep venous reflux
At diagnostic work-up (24 first hours following admission)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To compare demographic characteristics between groups of patients with and without a new episode of PE based on expert panel decision and lower limbs CDUS results.
Time Frame: At diagnostic work-up (24 first hours following admission)
Statistical analysis of the following characteristics based on demographic variables usually collected in our hospital during patient management : Age, gender, height, weight, BMI.
At diagnostic work-up (24 first hours following admission)
To compare clinical characteristics between groups of patients with and without a new episode of PE based on expert panel decision and lower limbs CDUS results.
Time Frame: At diagnostic work-up (24 first hours following admission)

Statistical analysis of the following characteristics based on clinical variables usually collected in our hospital during patient management :

  • Vital signs: temperature, systolic blood pressure, diastolic blood pressure, heart rate, peripheral oxygen saturation (%)
  • Clinical scores: diagnostic (Wells score), prognostic (sPESI, ESC)
  • Symptoms: dyspnea, chest pain, malaise, hemoptysis, lower limb edema, lower limb redness, lower limb pain
  • History of venous thromboembolic disease (details)
  • Context: presence or absence of risk factors for venous thromboembolic disease
  • Comorbidities: chronic respiratory failure, chronic heart failure, hemorrhagic or ischemic stroke, hypertension, dyslipidemia, smoking, cancer
  • Treatment: antiplatelet, anticoagulant, anti-inflammatory, hormonal treatment, chemotherapy
At diagnostic work-up (24 first hours following admission)
To compare biological characteristics between groups of patients with and without a new episode of PE based on expert panel decision and lower limbs CDUS results.
Time Frame: At diagnostic work-up (24 first hours following admission)

Statistical analysis of the following characteristics based on blood tests usually performed in our hospital during patient management :

  • Hemoglobin, neutrophil/lymphocyte ratio, D-dimer
  • Creatinine clearance expressed as Cockcroft and Gault (mL/min), CRP (mg/L)
  • NT-proBNP, troponin, fibrinogen
At diagnostic work-up (24 first hours following admission)
To compare imaging characteristics between groups of patients with and without a new episode of PE based on expert panel decision and lower limbs CDUS results.
Time Frame: At diagnostic work-up (24 first hours following admission)

Statistical analysis of the following characteristics based on imaging tests usually performed in our hospital during patient management :

  • CT pulmonary angiography
  • Ventilation-perfusion scan
  • Venous CDUS
At diagnostic work-up (24 first hours following admission)

Collaborators and Investigators

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

Investigators

  • Study Director: Marie ELIAS, MD, Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

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 (Actual)

March 4, 2022

Primary Completion (Actual)

November 4, 2023

Study Completion (Actual)

November 4, 2023

Study Registration Dates

First Submitted

June 7, 2022

First Submitted That Met QC Criteria

June 7, 2022

First Posted (Actual)

June 10, 2022

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 10, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Pulmonary Embolism

Clinical Trials on Color Doppler Ultrasound

Subscribe