MedTrace Logo

Pre-hospital Management of Aortic Dissection

NCT04304443 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2020-03-23

No results posted yet for this study

Summary

Background :

Time between symptoms onset and treatment initiation is crucial in Acute aortic dissection (AAD). An anti-hypertensive treatment can be rapidly initiated before the arrival in Emergency Department (ED). A better understanding of the chain of care between symptoms onset and surgery could lead to a reduction of morbi-mortality. Our study have the objective to describe the chain of care of patients with AAD in the ED.

Methods :

This is an observational, retrospective, multicenter study. Patients were detected with a discharge of diagnostic of aortic dissection (ICD I71.0) in university medical center of Besançon. Data collection : patients records in the 8 hospitals centers of the area Franche-Comté.

Conditions

  • Aortic Dissection

Sponsors & Collaborators

  • Hopital Nord Franche-Comte

    collaborator OTHER

  • Centre Hospitalier de Lons Le Saunier

    collaborator UNKNOWN

  • Centre hospitalier de Vesoul

    collaborator UNKNOWN

  • Centre hospitalier de Pontarlier

    collaborator UNKNOWN

  • Centre hospitalier de Gray

    collaborator UNKNOWN

  • Centre hospitalier de Dole

    collaborator UNKNOWN

  • Centre Hospitalier de Saint-Claude

    collaborator UNKNOWN

  • Centre Hospitalier Universitaire de Besancon

    lead OTHER

Principal Investigators

  • Christian Daguerre, MD-student · CHU de Besançon

  • Antoine Sigaux, MD · CHU de Besançon

  • Thibaut Desmettre, MD, PHD · CHU de Besançon

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-01
Primary Completion
2020-05-01
Completion
2020-07-01

Countries

  • France

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04304443 on ClinicalTrials.gov