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Clinical Trial Summary

- The purpose of this study is to evaluate the diagnostic accuracy of thoracic magnetic resonance imaging with gadolinium-enhanced, unenhanced and perfusion sequences in patients with clinically suspected acute pulmonary embolism

- Thoracic CT angiography (CTA) will serve as reference standard

- Result of MRI will not interfere with patients' management

- Untreated patients with negative CTA will have 3-month follow-up to verify they were free of thrombose-embolic disease


Clinical Trial Description

Background In patients with clinically suspected pulmonary embolism (PE)°with a contraindication to thoracic CT angiography, there is a need for an alternative diagnostic procedure. MRI has not been fully evaluated in this field; moreover, recent technological advances make it necessary to re-evaluate its performance for PE diagnosis.

Design Prospective monocentric study

- Patients with clinically suspected acute pulmonary embolism will undergo thoracic magnetic resonance imaging if inclusion criteria are fulfilled.

- A non-inclusion register will be establish for patients fulfilling the inclusion criteria , not included because MRI was not available (off-hours presentation , another patients already included in the protocol on the same day )

Estimated enrolment : 280 (based on a 25% prevalence of PE in our institution and an expected 80% sensitivity of MRI) Study start date: June 2007 Estimated study completion date: 17 months later (40 to 50 presentations for PE suspicion each month, 20 inclusions expected per month)

Magnetic Resonance imaging: performed on a 1.5 Tesla unit with 3 different sequences

- Unenhanced Steady State Free Precession (SSFP) sequences

- Perfusion imaging following Gadolinium injection at a rate of 5 c/s and a dose of 0.1mmol/kg

- Magnetic resonance angiography following an injection of 0.1mmol/kg of gadolinium at 3ml/s MRI studies will be interpreted secondarily by 2 independent radiologists, blinded to CTA results and clinical probability.

Two different readings will be performed, one global reading and one reading of each sequence separately, displayed in a random order (access base)

Objectives

- to evaluate MRI performance for PE diagnosis globally

- to evaluate the diagnostic value for each sequence (especially the negative predictive value of a normal perfusion sequence)

- to evaluate inter-observer agreement

MRI and CTA have to be performed within 24 hours ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01077778
Study type Observational
Source Assistance Publique - Hôpitaux de Paris
Contact
Status Terminated
Phase N/A
Start date March 2007
Completion date February 2010

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