- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02820909
Interest of the Ultrasound Guidance for the Laying of Femoral Arterial and Venous Catheters in Intensive Care Unit (ECHOGUIDE)
Interest of the Ultrasound Guidance for the Laying of Femoral Arterial and Venous Catheters in Intensive Care Unit: A Controlled, Randomized Trial: The ECHOGUIDE Study
The femoral approach is the preferred vascular access for the set-up of emergency catheters in severely traumatized patient. This location combines simplicity and speed of installation, it allows the simultaneous set-up of arterial and venous catheters, and is a provider of few complications and failures.
The ultrasound guidance has greatly reduced installation times, failures and complications related to the set-up of central venous catheter. This was amply demonstrated in the internal jugular and subclavian site outside of extreme emergency situations (Fragou M et al 2011, Farrell J et al 1997, Karakistos et al 2006). The benefit of ultrasound guidance for the set-up of arterial and venous catheters in the femoral emergency has not been evaluated in terms of reduction in complications.
Then the main objective of this study is to demonstrate that the ultrasound guidance reduces early complications related to the set-up of arterial and venous catheters in the femoral emergency, among severely traumatized patient compared to the reference anatomical technique.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Lyon, France, 69003
- Department of intensive care unit, Hospital Edouard Herriot- Hospices Civils de Lyon, 5 Place d'Arsonval
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult
- Included in intensive care unit for severe trauma
- Need for implementation of femoral arterial and venous catheters in accordance with the practices of the service.
- Agreed to participate
- Affiliation to national security
Exclusion Criteria:
- Contraindication to the set-up of vascular access in femoral position (femoral Scarpa wound, aortic dissection)
- Local infection
- Hypothermia <32°C
- Need for implementation of arterial catheter only
- Need for implementation of venous catheter only
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Ultrasound guidance
46 patients in the experimental ultrasound group
|
The insertion of the venous and arterial catheter will be done using ultrasound guidance.
Vein and artery will be identified in cross section.
In case of anatomical difficulties, complications of puncture with anatomical landmarks, or if installation time is greater than > 5 minutes, an intra-osseous catheter will be put in place to avoid delaying of treatment according to the current practice of the intensive care unit.
|
Active Comparator: Anatomical guidance
46 patients in the anatomical group
|
In the anatomical group, catheter will be inserted using, as it is currently done in intensive care unit, anatomic landmarks. If catheterization according to the anatomic method is considered too difficult (> 3 punctures), a conversion to ultrasound guidance will be done. In case of anatomical difficulties, complications of puncture with anatomical landmarks, or if installation time is greater than > 5 minutes, an intra-osseous catheter will be put in place to avoid delaying of treatment according to the current practice of the intensive care unit. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of complications 1 week after catheter set-up.
Time Frame: 1 week.
|
The primary end point is the proportion of patients with a complication one week after arterial and venous catheter set-up. Complications will be defined as follows:
Vascular assessment will be conducted by an angiologist, using doppler ultrasound of the femoral vessels. Assessment will be made blind from the use of ultrasound guidance during installation. |
1 week.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cannulation time between the 2 groups
Time Frame: the day of surgery (Day 1)
|
Comparison of cannulation mean time between the ultrasound guidance group and anatomical guidance group. Cannulation time is defined as the time in seconds, from the first contact between the needle and the skin, and when the two guide wires are inserted into the vessels (artery and vein). |
the day of surgery (Day 1)
|
total catheter set-up time between the 2 groups
Time Frame: the day of intervention (Day 1)
|
Comparison of total catheter set-up mean time between the ultrasound guidance group and anatomical guidance group. Total exposure time of the catheter is defined as the time, in seconds, from the first contact between the needle and the skin, and when the dressing is applied to both catheters in place and fixed. |
the day of intervention (Day 1)
|
Success of cannulation
Time Frame: the day of intervention (Day 1)
|
Comparison of cannulation success proportion at first attempt between the 2 groups.
Cannulation at first attempt is a success if the needle is inserted at first attempt.
A cannulation is defined as successful if the needle is inserted without resistance
|
the day of intervention (Day 1)
|
Number of cannulation attempt
Time Frame: the day of intervention (Day 1)
|
Comparison of the number of attempt before cannulation success in between the 2 groups.
Conversion to ultrasound guidance in the anatomical guidance group will be taken into account.
|
the day of intervention (Day 1)
|
Number of puncture attempt
Time Frame: day of intervention (Day 1)
|
Comparison of the total number of puncture between the 2 groups.
A puncture test is defined as the passage of the needle without changing direction or without new movement in depth.
Each needle withdrawal, followed by a new movement to deep planes or redirection of the needle is regarded as a new test, with or without skin puncture.
The number of tests will be evaluated by an observer.
|
day of intervention (Day 1)
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Aurelie MAZAUD, MD, Department of intensive care unit, Hospital Edouard Herriot- Hospices Civils de Lyon
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69HCL16_0403
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