Prevalence Rate of Pulmonary Embolism Among Not Anticoagulated Patients

NCT ID: NCT03525535

Last Updated: 2019-09-16

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

TERMINATED

Total Enrollment

1 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-06-14

Study Completion Date

2018-11-27

Brief Summary

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The purpose of this study is to evaluate the prevalence rate of pulmonary embolism among not anticoagulated patient older than 75 years old admitted with syncope and hospitalised in the Toulon Hospital

Detailed Description

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This study will be proposed to every patient that correspond to eligibility criteria. Will be included only those who are not opposed to the collection of their data.

The data collected will come from the routine care such as medical history, clinical datas, imaging data… The number of pulmonary imaging will be assessed before the diagnostic strategy proposed by Dr Prandoni and after the application of this strategy thanks to a questionnaire to physicians.

Conditions

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Pulmonary Embolism

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Pulmonary embolism

data from routine care will be collected for patient eligible and willing to participate

data collection

Intervention Type OTHER

data from patient included will be collected during the study

Interventions

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data collection

data from patient included will be collected during the study

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male or Female over 75 years-old
* Emergency consult resulting on an hospitalization in the geriatric service or in the internal medicine service
* Hospitalised in the Centre Hospitalier Intercommunal de Toulon for syncope, presenting these symptoms:
* Loss of consciousness with quick return to normal (less than one minute)
* Spontaneous resolution

Exclusion Criteria

* history of syncope
* other loss of consciousness (epilepsy, stroke, head trauma)
* anticoagulated treatment
* patient's objection
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Intercommunal de Toulon La Seyne sur Mer

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Benoit Faucher, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

Locations

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Centre Hospitalier Intercommunal Toulon La Seyne sur Mer

La Seyne-sur-Mer, Var, France

Site Status

Countries

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France

Other Identifiers

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2017-A01197-46

Identifier Type: OTHER

Identifier Source: secondary_id

2017-CHITS-04

Identifier Type: -

Identifier Source: org_study_id

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