- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01122693
Comparison Between Two Ultrasound Technologies for Ultrasound-guided Catheter Placement in Regional Anesthesia (eZono)
A Prospective, Randomized Comparison Between Two Ultrasound Technologies for Ultrasound-guided Catheter Placement in Regional Anesthesia
The use of ultrasound imaging techniques in regional anaesthesia is rapidly becoming an area of increasing interest. It represents one of the largest changes that the field of regional anaesthesia has seen. For the first time, the operator is able to view an image of the target nerve directly, guide the needle under real-time observation, navigate away from sensitive anatomy, and monitor the spread of local anaesthetic (LA).The key to successful regional anaesthesia is deposition of LA accurately around the nerve structures.
In the past, electrical stimulation which relied on surface landmark identification, was used for this. However, landmark techniques have limitations; variations in anatomy and nerve physiology , as well as equipment accuracy have had an effect on success rates and complications.
However, alongside the enthusiasm of ultrasound guidance in regional anaesthesia, there should be a degree of informed scepticism. The widespread use of the various techniques of ultrasound-guided regional blocks without adequate training raises the danger of malpractice and subsequent impaired outcome.
Adequate education in the use of regional block techniques under ultrasound guidance is essential. Recent technical developments have achieved higher ultrasound frequencies and better image resolution, as well as better post-processing and user-friendliness.
The purpose of this study is to determine whether new technical features such as reference images, higher ultrasound frequencies, better image resolution and smaller size and weight of the ultrasound probes may improve outcome (clinical benefits) and may show an increased efficacy and safety. And if the new technology of ultrasound images improves the training quality of trainees and novices in the art of ultrasound-guided blocks.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Berlin, Germany, 10117
- Charité - Universitätsmedizin Berlin, Klinik für Anästhesiologie
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Berlin, Germany, 10117
- Department of Anesthesiology and Operative Intensive Care Medicine Campus Charité Mitte / Campus Virchow-Klinikum
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients at the age of 18 and above who need a regional anesthesia catheter for postoperative pain management after elective orthopedic surgery
Exclusion Criteria:
- Participation in another trial according to the German Drug Law 30 days to and during the study
- Lacking willingness to save and hand out data within the study
- Accommodation in an institution due to an official or judicial order
- (Unclear) history of alcohol or substances disabuse
- Absent knowledge of German language
- Analphabetism
- Allergy to local anesthesia or other ingredients of the intravenous solutions
- For women: Pregnancy or positive pregnancy test within the preoperative screening
- Operation due to case of emergency, polytrauma or pathologic fracture
- American Society of Anaesthesiologists (ASA) classification greater than III
- Peripheral or central edema
- AIDS (according to the CDC-classification of HIV-infection: category C)
- Immunosuppression therapy
- History of bleeding tendency (e.g. von-Willebrand-disease, thrombocytopenia)
- Derailed metabolic disorder (e.g. Diabetes mellitus (Glucose > 300 mg/dl) during the preoperative screening)
- Known history of electrolyte disturbance (e.g. Hyperkalemia > 5.8 mmol/l, Hypernatraemia > 155 mmol/l)
- Known history of acid-base-dysbalances
- History of intracranial hemorrhage within one year of participation in the study
- Neurological or psychiatric disease with limited contractual capability
- CHF (congestive heart failure) according to (New York Heart Association) classification - NYHA class IV
- Liver disease (CHILD B or C cirrhosis, end-stage liver disease (MELD-score greater than 10)
- Renal insufficiency (serum creatinine greater than 2.0 mg/dl or greater than 150 µmol/l or dependency of haemodialysis)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: standard 2D ultrasound images
|
higher ultrasound frequencies, better image resolution, better post-processing and user-friendliness.
current standard in two-dimensional (2D) ultrasound images
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Experimental: high-quality 2D ultrasound images
|
higher ultrasound frequencies, better image resolution, better post-processing and user-friendliness.
current standard in two-dimensional (2D) ultrasound images
|
Active Comparator: nerve stimulation techniques
|
higher ultrasound frequencies, better image resolution, better post-processing and user-friendliness.
current standard in two-dimensional (2D) ultrasound images
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Reduction in time to perform the catheter placement in regional anesthesia
Time Frame: first three days
|
first three days
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Improvement in performance: Incidence of complications
Time Frame: first three days
|
first three days
|
Improvement of success rate regarding correct catheter placement
Time Frame: first three days
|
first three days
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
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 (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- eZono
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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