Efficacy of the echOpen Device to Identify Effusion and to Detect Basilic Vein (CLIN-ECHO-I)
Pleural Effusion, Abdominal Effusion, Procedural Guidance
About this trial
This is an interventional screening trial for Pleural Effusion focused on measuring Ultrasound, Ultrasonography, Point-of-care-ultrasound, Pleural Effusion, Abdominal Effusion, Basilic vein
Eligibility Criteria
Inclusion Criteria:
- Adult patient (age ≥ 18 years old)
- Patient having signed the informed consent to participate in this clinical investigation
- Patient affiliated to the social security scheme
- Patient arriving in the hospital clinical ward (own initiative or by emergency services) whose clinical symptomatology (e.g. dyspnea, thoracic pain, etc.) suggests the presence of pathological elements (effusion) which would be visible using an ultrasound probe
- Patient consulting in the hospital clinical ward who could potentially benefit from a basilic vein line placement using an ultrasound device
Exclusion Criteria:
- Minor patient (age < 18 years)
- Patients under the "State medical assistance"
- Obese patient (body mass index > 29.9)
- Patient in too serious condition for the clinical examination to be done fully and/or with additional exploratory time
- Unstable patient: need for immediate care, impossibility to carry out a thorough clinical examination including interview, palpation, auscultation, percussion
- Known allergy to ultrasound gel
Sites / Locations
- Avicenne Hospital - APHP - Hepatology Department
- Cochin Hospital - APHP - Emergency Department
- Cochin Hospital - APHP - Pneumology department
- Paul Brousse Hospital - APHP - Hepatobiliary Center
Arms of the Study
Arm 1
Experimental
Patients benefitting ultrasound examination
This is the only arm of the study. Patients with an indicative clinical picture that leads the clinician to resort to the use of an ultrasound to potentially support the diagnosis will be examined to verify the presence of pleural effusion or intra-abdominal effusion, or to identify basilic vein. The patients will be assessed first with the echOpen device and second witn an ultrasound routinely used in the department. In a case of discordance between the assessments made with echOpen and the usual ultrasound device, an independent referent radiologist will use a standard ultrasound machine to constitute the gold standard (GS) rating