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Diagnostic Value of Portable Ultrasound for Dyspneic Patient Support in the Emergency Department (VSCAN-DYSP)

C

Centre Hospitalier Universitaire de Nīmes

Status

Terminated

Conditions

Dyspnea

Treatments

Other: Standard care
Device: Vscan portable ultrasound device (GE Healthcare, Wauwatosa, WI)

Study type

Interventional

Funder types

Other

Identifiers

NCT01818882
2013-A00100-45 (Other Identifier)
LOCAL/2012/XB-01

Details and patient eligibility

About

The main objective of our study is to compare the effects of two care strategies for dyspneic patients on the length of hospital stay: (1) standard care (=contextual analysis + conventional clinical chest radiography) versus (2) standard care + pleuropulmonary ultrasound.

Full description

The secondary objectives of this study are to assess the following for both arms:

A-fatality rate, B-degree of concordance between the diagnosis orientation in the emergency department and final diagnosis determined by an expert committee using patient records one month later (blind evaluation by a panel of experts) C-clinical improvement between early emergency care and later care outside the emergency department (clinical parameters = blood gases and other biological parameters) D-imaging parameters.

Enrollment

85 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • The patient must have given his/her informed and signed consent
  • The patient must be insured or beneficiary of a health insurance plan
  • Patient consulting in the emergency department for dyspnea

Exclusion criteria

  • The patient is participating in another study
  • The patient is in an exclusion period determined by a previous study
  • The patient is under judicial protection, under tutorship or curatorship
  • The patient refuses to sign the consent
  • It is impossible to correctly inform the patient
  • The patient cannot read French
  • The patient is pregnant, parturient, or breastfeeding

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

85 participants in 2 patient groups

Standard care
Active Comparator group
Description:
Patients randomized to this arm will receive standard care. Intervention: Standard care.
Treatment:
Other: Standard care
Standard care + ultrasound
Experimental group
Description:
Patients randomized to this arm will receive standard care + pleuropulmonary ultrasound. Intervention: Standard care + ultrasound
Treatment:
Device: Vscan portable ultrasound device (GE Healthcare, Wauwatosa, WI)
Other: Standard care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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