NCT00771303

Brief Summary

Venous thromboembolism (VTE) remains a major cause of maternal morbidity and mortality in developed countries. Objective diagnosis of pulmonary embolism (PE) and/or deep vein thrombosis (DVT) in pregnancy is crucial. Failure to identify PE or/or DVT will place the mother's life at risk, and unnecessary treatment will not only expose her to anticoagulants but will also label her as having had VTE. Thus, this diagnosis has serious implications for the management of her present pregnancy, and for other aspects of her life ranging from contraception to thromboprophylaxis in future pregnancies and hormone replacement therapy in later life. It is therefore critical that all women with symptoms or signs that suggest venous thromboembolism have appropriate investigation and diagnosis based on objective diagnostic tests. The current diagnostic approach in suspected PE is based on sequential diagnostic tests: 1) assessment of clinical probability, 2) fibrin D-dimer measurement, 3) compression ultrasonography of lower limb veins and 4) multi-slice computed tomography (MSCT). However, physicians are reluctant to perform MSCT in pregnant women because of potential adverse effect of radiation exposure to the fetus. For this reason, ventilation/perfusion or perfusion-only lung scan has been the cornerstone of PE diagnosis in pregnant women. Indeed, perfusion lung scan was assumed to be associated with less radiation than computed tomography (CT). However, this technique is now widely abandoned in the usual diagnostic strategy of PE for the following reasons: it is not widely available; its interpretation may be difficult and the test may be inconclusive in the presence of other chest abnormalities. Moreover, recent data convincingly show that the radiation exposure associated with single-slice or multi-slice CT exposes the fetus to less radiation than perfusion lung scan. However, the use of CT has never been adequately validated in pregnant women with clinically suspected PE. The investigators, therefore, plan to set up a prospective management study in which pregnant women with suspected PE will undergo a sequential diagnostic strategy based on 1) assessment of clinical probability 2) D-dimer measurement 3) compression ultrasonography, and 4) MSCT. Nowadays, the overestimated fear of radiation exposure for the fetus leads to an irrational attitude and inadequate investigations in pregnant women with suspected PE, even though both European \[3, 4\] and North-American guidelines \[5\] suggest that only objective testing may accurately rule out the disease. The proposed study should lead to an increased awareness of the risks and benefits of appropriate imaging in pregnant women suspected of PE and should result in a more rational management of this under-studied patient group.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
402

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2008

Longer than P75 for all trials

Geographic Reach
2 countries

9 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2008

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

October 10, 2008

Completed
3 days until next milestone

First Posted

Study publicly available on registry

October 13, 2008

Completed
8.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2017

Completed
Last Updated

May 9, 2018

Status Verified

May 1, 2018

Enrollment Period

8.9 years

First QC Date

October 10, 2008

Last Update Submit

May 3, 2018

Conditions

Keywords

PregnancyPulmonary embolismMSCT

Outcome Measures

Primary Outcomes (1)

  • Proportion of patients with a symptomatic thromboembolic event in the three month follow-up among those in whom PE was ruled out by the diagnostic strategy and who were left untreated by anticoagulants.

    3 months

Secondary Outcomes (3)

  • Efficacy of non invasive testing

    3 months

  • Proportion of patients with a negative D-dimer result

    3 months

  • Proportion of patients with a lower limb venous ultrasound showing a proximal DVT

    3 months

Study Arms (1)

Ct scan

Pregnant patients with suspected PE will undergo a strategy based on clinical probability assessment, D-dimer measurement, lower limb compression ultrasonography and multi-slice computed tomography.

Other: Pregnant patients with suspected PE will undergo a strategy based on clinical probability assessment, D-dimer, lower limb vein ultrasonography and MSCT.

Interventions

Eligibility Criteria

Age18 Years - 50 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Pregnant women with suspected PE.

You may not qualify if:

  • Age less than 18 years
  • Absence of informed consent
  • Patients allergic to contrast medium
  • Impaired renal function (creatine clearance less than 30 ml/min as estimated by the Cockroft formula)
  • Geographic inaccessibility for follow-up

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (9)

Pierre-Marie ROY

Angers, 49933, France

Location

Grégoire LE GAL

Brest, 29609, France

Location

Florence PARENT

Clamart, 92141, France

Location

Isabelle QUERE

Montpellier, 34295, France

Location

Jean-Christophe GRIS

Nîmes, 30029, France

Location

Guy MEYER

Paris, 75015, France

Location

Caroline BOHEC

Pau, 64000, France

Location

Antoine ELIAS

Toulon, 83056, France

Location

Marc Righini

Geneva, 1205, Switzerland

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Nt-pro BNP measurement

MeSH Terms

Conditions

Pulmonary EmbolismVenous Thrombosis

Interventions

fibrin fragment D

Condition Hierarchy (Ancestors)

Lung DiseasesRespiratory Tract DiseasesEmbolismEmbolism and ThrombosisVascular DiseasesCardiovascular DiseasesThrombosis

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof

Study Record Dates

First Submitted

October 10, 2008

First Posted

October 13, 2008

Study Start

September 1, 2008

Primary Completion

August 1, 2017

Study Completion

August 1, 2017

Last Updated

May 9, 2018

Record last verified: 2018-05

Locations