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Efficacy of the echOpen Device to Identify Effusion and to Detect Basilic Vein (CLIN-ECHO-I)

Primary Purpose

Pleural Effusion, Abdominal Effusion, Procedural Guidance

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
EchOpen ultra-portable ultrasound device
Ultrasound device routinely used in the department.
Standard ultrasound examination by an independent referent radiologist
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Arm Label

Patients benefitting ultrasound examination

Arm Description

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

Outcomes

Primary Outcome Measures

Presence of Pleural effusion
Presence or absence of pleural effusion as assessed by the echOpen device or by a portable ultrasound routinely used in the department
Presence of Intra-abdominal effusion
Presence or absence of intra-abdominal effusion as assessed by the echOpen device or by a portable ultrasound routinely used in the department
Basilic vein identification
Successful identification of the basilic vein using the echOpen device or a portable ultrasound routinely used in the department

Secondary Outcome Measures

Plural effusion detected using a gold standard procedure
Presence of pleural effusion determined by an independent referent radiologist using a standard ultrasound machine
Intra-abdominal effusion detected using a gold standard procedure
Presence or absence of intra-abdominal effusion determined by an independent referent radiologist using a standard ultrasound machine
Basilic vein identification using a gold standard procedure
Identification of the basilic vein by an independent referent radiologist using a standard ultrasound machine

Full Information

First Posted
March 4, 2022
Last Updated
December 7, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
ECHOPEN, EIT Health
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1. Study Identification

Unique Protocol Identification Number
NCT05280119
Brief Title
Efficacy of the echOpen Device to Identify Effusion and to Detect Basilic Vein
Acronym
CLIN-ECHO-I
Official Title
Assessment of the echOpen Ultra-portable Ultrasound Device in Daily Use by Clinicians. Part I: Identification of Effusion and Detection of Basilic Vein
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
April 4, 2022 (Actual)
Primary Completion Date
August 19, 2022 (Actual)
Study Completion Date
August 19, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
ECHOPEN, EIT Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In recent years, portable and ultra-portable ultrasound devices are increasingly used by the non radiologists, notably cardiologists or obstetrician gynecologist, at the patient's bedside to visualize and measure anatomical structures and fluid and provide the clinical examination with additional signs allowing quicker and more confident clinical decisions. This innovative approach is slowed down by the accessibility of these miniaturized devices, the price of which remains high. The echOpen device includes an ultra-portable ultrasound probe and a mobile application that allows the image to be displayed on a smartphone via a WIFI protocol. The objective of the clinical investigation is to show that the echOpen device, using three frequencies 3.5 Mhz, 5.0 Mhz and 7.5 Mhz, allows identifying the semiological signs or anatomical structures of interest located at several depths of the body, with a performance similar to other devices routinely used in clinical departments.
Detailed Description
The echOpen device includes an ultrasound probe and a mobile application. The mechanical probe emits at three ultrasound frequencies, 3.5 Mhz, 5.0 Mhz and 7.5 Mhz, which allows the exploration of the interior of the body at different depths in a non-invasive and non-irradiating manner. Thus, the purpose of the echOpen device is, on one hand, to guide the diagnosis during the clinical examination and, on the other hand, to identify anatomical structures in order to assist in management. The objective of the clinical investigation is to demonstrate that the echOpen device is able to identify semiological signs and localize anatomical structures at different depths of the body, with a performance not inferior to that of other ultrasound devices, routinely employed in hospital clinical departments. The signs of interest (i.e. search for an intra-abdominal (3.5 Mhz) and pleural (5.0 Mhz) effusion) were chosen for their clinical usefulness (their presence during the clinical examination constitutes an argument for orientation and/or severity) and for their prevalence in the study population. The identification of anatomical structure of interest (i.e. detection of basilic vein (7.5Mhz)) was chosen because it is a gesture frequently used when taking in charge of a patient hospitalized in the selected departments. An ultrasound probe in use in the hospital clinical departments where the investigation takes place will be employed as a comparator to judge the performance of the echOpen device. This clinical investigation is part of a CE marking procedure.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pleural Effusion, Abdominal Effusion, Procedural Guidance
Keywords
Ultrasound, Ultrasonography, Point-of-care-ultrasound, Pleural Effusion, Abdominal Effusion, Basilic vein

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A single group, comparative, non-randomized, controlled study. Each patient represents her/his own control: the patient is examined consecutively with the echOpen probe, then with the probe used in the department
Masking
None (Open Label)
Masking Description
Open Label
Allocation
N/A
Enrollment
201 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Patients benefitting ultrasound examination
Arm Type
Experimental
Arm Description
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
Intervention Type
Device
Intervention Name(s)
EchOpen ultra-portable ultrasound device
Intervention Description
Depending on the clinical picture, patients are examined to detect the presence or absence of pleural effusion, or intra-abdominal effusion, or to localize the basilic vein
Intervention Type
Device
Intervention Name(s)
Ultrasound device routinely used in the department.
Intervention Description
Patients who were first examined with the EchOpen ultra-portable ultrasound device, are secondarily examined with an ultrasound probe used routinely in the department.
Intervention Type
Procedure
Intervention Name(s)
Standard ultrasound examination by an independent referent radiologist
Intervention Description
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
Primary Outcome Measure Information:
Title
Presence of Pleural effusion
Description
Presence or absence of pleural effusion as assessed by the echOpen device or by a portable ultrasound routinely used in the department
Time Frame
Day 0
Title
Presence of Intra-abdominal effusion
Description
Presence or absence of intra-abdominal effusion as assessed by the echOpen device or by a portable ultrasound routinely used in the department
Time Frame
Day 0
Title
Basilic vein identification
Description
Successful identification of the basilic vein using the echOpen device or a portable ultrasound routinely used in the department
Time Frame
Day 0
Secondary Outcome Measure Information:
Title
Plural effusion detected using a gold standard procedure
Description
Presence of pleural effusion determined by an independent referent radiologist using a standard ultrasound machine
Time Frame
Day 0
Title
Intra-abdominal effusion detected using a gold standard procedure
Description
Presence or absence of intra-abdominal effusion determined by an independent referent radiologist using a standard ultrasound machine
Time Frame
Day 0
Title
Basilic vein identification using a gold standard procedure
Description
Identification of the basilic vein by an independent referent radiologist using a standard ultrasound machine
Time Frame
Day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jérôme BOKOBZA, MD
Organizational Affiliation
AP-HP, Cochin Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Avicenne Hospital - APHP - Hepatology Department
City
Bobigny
ZIP/Postal Code
93140
Country
France
Facility Name
Cochin Hospital - APHP - Emergency Department
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Cochin Hospital - APHP - Pneumology department
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Paul Brousse Hospital - APHP - Hepatobiliary Center
City
Villejuif
ZIP/Postal Code
94800
Country
France

12. IPD Sharing Statement

Learn more about this trial

Efficacy of the echOpen Device to Identify Effusion and to Detect Basilic Vein

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