ECHO_NCMB: Ultrasound-guided Versus Blind Technique in Medial Brachial Cutaneous Nerve and Intercostobrachial Nerve Blocks
Study Details
Study Description
Brief Summary
The axillary brachial plexus block is a technique of locoregional anesthesia indicated in the distal upper limb surgery : hand, forearm, the lower third of the arm including the elbow. The anesthesia of the posterior and the medial side of the arm requires a selective block of the medial brachial cutaneous nerve and the intercostobrachial nerve, for example to improve the tolerance of the inflatable tourniquet used by the surgeons. There are two techniques to achieve this block : the blind technique (without ultrasound) and the ultrasound-guided technique. At the moment, there are no studies which compare these two techniques. So, the purpose of this study is to determine the effectiveness of ultrasound-guided technique compared to blind technique in medial brachial cutaneous nerve block and intercostobrachial nerve block, in the axilla.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
For purposes of this single-blind monocentric study, 84 patients are randomized into two groups (42 patients for each), upon enrolment into the study.
In the first group, the blind technique is used to perform the medial brachial cutaneous nerve block and the intercostobrachial nerve block : it consists in performing a subcutaneous injection of the local anesthetic at the root of the arm, in the anterior-posterior direction.
In the second group, the ultrasound-guided technique is used to perform the medial brachial cutaneous nerve block and the intercostobrachial nerve block : ultrasounds are used to visualize the anatomical variations, the good position of the needle and the good local anesthetic diffusion.
The aim is to evaluate the effectiveness of ultrasound-guided technique compared to blind technique in medial brachial cutaneous nerve block and intercosto-brachial nerve block, in the axilla
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: blind technique Investigators will perform a medial brachial cutaneous nerve block and an intercostobrachial nerve block with either a blind technique or an ultrasound-guided technique to estimate the effectiveness of each technique. The blind technique consists in performing a subcutaneous injection of the local anesthetic at the root of the arm, in the anterior-posterior direction. |
Procedure: medial brachial cutaneous nerve block and intercostobrachial nerve block with blind technique
It consists in performing a subcutaneous injection of the local anesthetic at the root of the arm, in the anterior-posterior direction.
|
| Active Comparator: ultrasound-guided technique Investigators will perform a medial brachial cutaneous nerve block and an intercostobrachial nerve block with either a blind technique or an ultrasound-guided technique to estimate the effectiveness of each technique. In the ultrasound-guided technique, ultrasounds are used to visualize the anatomical variations, the good position of the needle and the good local anesthetic diffusion. |
Procedure: medial brachial cutaneous nerve block and intercostobrachial nerve block with ultrasound-guided technique
Ultrasounds are used to visualize the anatomical variations, the good position of the needle and the good local anesthetic diffusion.
|
Outcome Measures
Primary Outcome Measures
- Number of participants with complete anesthesia in the lower half of the medial cutaneous area of the arm, at time 20 minutes [at time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block]
At time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block, a light touch sensitivity test is performed
- Number of participants with complete anesthesia in the upper half of the medial cutaneous area of the arm, at time 20 minutes [at time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block]
At time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block, a light touch sensitivity test is performed
- Number of participants with complete anesthesia in the lower half of the posterior cutaneous area of the arm, at time 20 minutes [at time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block]
At time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block, a light touch sensitivity test is performed
- Number of participants with complete anesthesia in the upper half of the posterior cutaneous area of the arm, at time 20 minutes [at time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block]
At time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block, a light touch sensitivity test is performed
- Number of participants with complete anesthesia of the arm at time 20 minutes [at time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block]
At time 20 minutes after the achievement of medial brachial cutaneous nerve block and intercostobrachial nerve block, a light touch sensitivity test is performed
Secondary Outcome Measures
- Number of participants with complete anesthesia, with reduced sensitivity and with absence of anesthesia at times 5, 10, 15, 20 minutes (except primary outcome) in the areas of the medial brachial cutaneous nerve and the intercostobrachial nerve [at times 5, 10, 15, 20 minutes after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
- Number of patients with comfortable feeling, with unpleasant sensations and with pains during surgery, in the areas of the medial brachial cutaneous nerve and the intercostobrachial nerve (questionnaire completed by the anesthesist) [3 hours after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
- The total volume (mL) of local anesthetic used for the medial brachial cutaneous nerve block and the intercostobrachial nerve block [5 minutes after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
- Number of participants (of the ultrasound-guided group) with good ultrasound view of theses nerves before and after the injection of the local anesthetic [5 minutes after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
- Number of participants (of the ultrasound-guided group) with : bad ultrasound view of theses nerves before the injection and good ultrasound view of theses nerves after the injection of the local anesthetic [5 minutes after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
- Number of participants (of the ultrasound-guided group) with bad ultrasound view of theses nerves before and after the injection of the local anesthetic. [5 minutes after the achievement of the medial brachial cutaneous nerve block and the intercostobrachial nerve block]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Adult patients ≥ 18 years
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Surgery of the distal upper limb : hand, forearm, lower third of the arm ,including the elbow
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Urgent or planned surgery
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Locoregional anesthesia : axillary brachial plexus block, completed by a medial brachial cutaneous nerve block and an intercostobrachial nerve block
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Local anesthetic used : mepivacaine 10mg/ml
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In the absence of patient objections
Exclusion Criteria:
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Pregnancy
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Adults under guardianship
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Locoregional anesthesia contraindications
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Local anesthetic used : ropivacaine 0,75%
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Chru Nancy | Nancy | France | 54035 |
Sponsors and Collaborators
- Central Hospital, Nancy, France
Investigators
- Study Director: Hervé BOUAZIZ, Professor, CHU Nancy
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2016-A01296-45