US-SCBPB: Comparison 1 Plane-2 Injection and 2 Plane-2 Injection Ultrasound-guided Supraclavicular Brachial Plexus Block

Sponsor
Gachon University Gil Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT02533557
Collaborator
(none)
70
1
2
4
17.5

Study Details

Study Description

Brief Summary

The supraclavicular block can provide effective surgical anesthesia of the forearm and hand. There have been many different approaches to ultrasound-guided supraclavicular brachial plexus block (US-SCBPB) according to the needle injection site (e.g. corner pocket approach, cluster approach) or number of needling (single or double injection). Numerous studies demonstrates good results (e.g. faster onset time) when using double injections rather than single injection. But double injection does not guarantee complete sensory block because ulnar nerve tends to be spared by its anatomical location.

Condition or Disease Intervention/Treatment Phase
  • Device: stimuplex insulated needle
  • Drug: lidocaine mixed with epinephrine
N/A

Detailed Description

The investigators hypothesized that double injection in different plane (we call this new approach as a 2 plane-2 injection approach;2P2I) would overcome the weakness of the existing double injection in same plane (we call this approach as a 1 plane-2 injection approach;1P2I) like "ulnar nerve sparing effect", and could have a good results (e.g. shortening the onset time or increasing rate of all four nerves block). Because 2P2I can achieve an effect of a "tridimensionally administered LA", rather 1P2I only achieve an effect of a " two-dimensionally administered LA".

Study Design

Study Type:
Interventional
Actual Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Official Title:
A Randomized Comparison Between 1 Plane-2 Injection and 2 Plane-2 Injection Ultrasound-guided Supraclavicular Brachial Plexus Block (US-SCBPB) in Upper Extremity Surgery
Study Start Date :
Aug 1, 2015
Actual Primary Completion Date :
Dec 1, 2015
Actual Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: 2P2I group

subcutaneous injection is done widely. A nerve stimulating needle (Stimuplex insulated needle; D Plus B. Braun, Melsungen, Germany) attached to a nerve stimulator (Stimuplex HNS12; B. Braun, Melsungen, Germany) is advanced via an ultrasound in-plane approach. After the needle is penetrated the nerve sheath with a direction of downward, the nerve stimulator is then turned on. If hand muscle twitching is observed even at 0.3 mA, LA 15 mL (lidocaine mixed with epinephrine) is injected. After that, the stimulating needle is re-advanced at the behind site of the initial puncture site. And the needle is penetrated the nerve sheath with a direction of upward, and then the same process is performed and LA 15 mL is injected.

Device: stimuplex insulated needle
2P2I group: nerve stimulating needle is advanced twice with the up-down direction at the different puncture site and LA is injected 15 mL at a time. 1P2I group: nerve stimulating needle is advanced twice with the up-down direction at the same puncture site and LA is injected 15 mL at a time.
Other Names:
  • D Plus B.Braun
  • Drug: lidocaine mixed with epinephrine
    2P2I group and 1P2I group use the same LA (1.5% lidocaine mixed with 1:200,000 epinephrine). But 2P2I group is injected LA at equally divided doses (15 mL at a time) with the up-down direction at the different puncture site. 1P2I group is injected LA at equally divided doses with the up-down direction at the same puncture site.
    Other Names:
  • 1.5% lidocaine mixed with 1:200,000 epinephrine
  • Active Comparator: 1P2I group

    subcutaneous injection is done widely. A nerve stimulating needle (Stimuplex insulated needle; D Plus B. Braun, Melsungen, Germany) attached to a nerve stimulator (Stimuplex HNS12; B. Braun, Melsungen, Germany) is advanced via an ultrasound in-plane approach. After the needle is penetrated the nerve sheath with a direction of downward, the nerve stimulator is then turned on. If hand muscle twitching is observed even at 0.3 mA, LA 15 mL (lidocaine mixed with epinephrine) is injected. After that, the stimulating needle is re-advanced with a direction of upward at the same puncture site and penetrated the nerve sheath. If hand muscle twitching is observed at 0.3 mA, LA 15 mL is injected.

    Device: stimuplex insulated needle
    2P2I group: nerve stimulating needle is advanced twice with the up-down direction at the different puncture site and LA is injected 15 mL at a time. 1P2I group: nerve stimulating needle is advanced twice with the up-down direction at the same puncture site and LA is injected 15 mL at a time.
    Other Names:
  • D Plus B.Braun
  • Drug: lidocaine mixed with epinephrine
    2P2I group and 1P2I group use the same LA (1.5% lidocaine mixed with 1:200,000 epinephrine). But 2P2I group is injected LA at equally divided doses (15 mL at a time) with the up-down direction at the different puncture site. 1P2I group is injected LA at equally divided doses with the up-down direction at the same puncture site.
    Other Names:
  • 1.5% lidocaine mixed with 1:200,000 epinephrine
  • Outcome Measures

    Primary Outcome Measures

    1. rate of complete sensory blockade of all 4 nerves [check 30 minutes after performing the block at 5-minute intervals (from date of randomization until the date of first documented progression)]

      If the sensory on the site under the control of all 4 (median, radial, ulnar, musculocutaneous) nerves is checked as 0 (just feeling of touch or none ) separately, it is considered as a complete sensory block. the investigators compare the rate of complete sensory block with 2P2I group and 1P2I group.

    Secondary Outcome Measures

    1. the onset time [check 30 minutes after performing the block at 5-minute intervals(from date of randomization until the date of first documented progression)]

      The investigators compare the onset time (time required to obtain of a sensory block at the surgical incision site) with 2P2I group and 1P2I group.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • all patients anticipating surgery of the wrist or hand

    • age: 18 to 80 years

    • American Society of Anesthesiologists physical status (ASA): I or II

    Exclusion Criteria:
    • neuropathy in the operated limb

    • ASA greater than III

    • coagulation disorders

    • known allergy to local anesthetics

    • local infection at the puncture site

    • chronic obstructive pulmonary disease or respiratory failure

    • pregnancy or breast-feeding

    • prior surgery in the supraclavicular region

    • BMI ≥ 35 kg/㎡

    • uncooperative patients

    • patients' refusal

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Anesthesiology and Pain Medicine, Gachon University Gil Medical Center Incheon Guwol-dong, Namdong-gu Korea, Republic of 405-760

    Sponsors and Collaborators

    • Gachon University Gil Medical Center

    Investigators

    • Principal Investigator: Mi Geum Lee, MD, PhD, Gachon University Gil Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Mi Geum Lee, assistant professor, Gachon University Gil Medical Center
    ClinicalTrials.gov Identifier:
    NCT02533557
    Other Study ID Numbers:
    • GBIRB2015-45
    First Posted:
    Aug 27, 2015
    Last Update Posted:
    May 20, 2016
    Last Verified:
    May 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Mi Geum Lee, assistant professor, Gachon University Gil Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 20, 2016