Improvement of Needle Visibility in Ultrasound Guided Regional Anaesthesia

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01583010
Recruitment Status : Unknown
Verified April 2012 by Reinhard Hahn, Medical University of Vienna.
Recruitment status was:  Recruiting
First Posted : April 23, 2012
Last Update Posted : April 23, 2012
Information provided by (Responsible Party):
Reinhard Hahn, Medical University of Vienna

April 20, 2012
April 23, 2012
April 23, 2012
December 2011
May 2012   (Final data collection date for primary outcome measure)
Time of needle visibilty in ultrasound-image [ Time Frame: At time of ultrasound guided regional anaesthesia ]
Measure is given in percentage of procedure time
Same as current
No Changes Posted
  • Procedure time [ Time Frame: At time of ultrasound guided regional anaesthesia ]
    Duration of placement of the ultrasound probe up to needle-removal out of the skin.
  • Angle of needle insertion [ Time Frame: At time of ultrasound guided regional anaesthesia ]
    Measurement of puncture-angle between skin an needle in the ultrasound-image.
Same as current
Not Provided
Not Provided
Improvement of Needle Visibility in Ultrasound Guided Regional Anaesthesia
Improvement of Needle Visibility in In-line Regional Anaesthesia by "Advanced Needle Visualization Technology ®"

Needle tip visualization, although fundamental to the safety and efficacy of ultrasound-guided regional anesthesia (UGRA), can be extremely challenging. This problem is most marked at steep insertion angles. Studies in patients with UGRA demonstrate that echogenic needle designs have the potential to offer improved visibility and accuracy.

Our study pursues another approach. We use (for differentiation) echogenic nerve block needles with ANV®, a new SonoSite software-upgrade (Advanced Needle Visualization Technology®). We will compare UGRA with ANV® against standard UGRA without using this SonoSite software-upgrade. Patients undergoing femoral, supraclavicular or other nerve blocks as part of their routine anesthetic management are included.

This work represents the first randomized controlled double blinded clinical trial of ANV® in patients undergoing UGRA. We hypothesize, that we can decrease the time without needle visualization (Loss of needle time in percentage of procedure time) during in-line regional anaesthesia. Furthermore we will record quality of visibility, duration of procedure and insertion angle of the needle.

Patients scheduled to undergo surgery with femoral (n = 50) and supraclavicular (n=50) anaesthesia (100 blocks total) gets included in this study. These 50 patients will be randomized equally using sealed opaque envelopes to two parallel groups: standard treatment UGRA (n=25) and SonoSites ANV® (n= 25) UGRA.

An experienced anaesthesiologist from department of anaesthesiology, general intensive care and pain medicine will perform UGRA. Because of safety reasons and best assessment of needle visibility all UGRA in this study are going to performed with in-plane ultrasound technique. Needle length and gauge are standardized.

The ultrasound imaging of each nerve block gets recorded onto a DVD for analysis. Recording of performed UGRA will start with placement of ultrasound probe and will finish with needle leaving the skin (procedure time), get stored, checked to exclude technical failures and analysed with a one second discrimination by two blinded observers for needle visibility. All information indicating ANV®-status on ultrasound image will be deleted. Hence for procedure and following analysis we will ensure that patient and the objective observer are blinded.

Images with full needle visibility will be related to images without needle visibility. Time of needle visibility will be described in percent of procedure time.

Enduring visualization of complete needle in ultrasound beam won't be given during the whole procedure. For differentiation of complete needle visibility, partial or no visibility in in-plane UGRA, we will use needles with ultrasound visible marks (echogenic needles). If the objective observers will visualize all 3 marks and pole of the needle in ultrasound-image, needle is completely in-plane and visible for analysis. For partial visibility of marks we will use a needle visibility grading dependent to number of visible marks (One mark = poor visibility, two marks = middle visibility, three marks=good visibility). If there won't be visible marks in ultrasound image, needle is in absence and gets evaluated as "not visible".

Dependent to position of anatomic target structure each nerve block will need a different angle of needle insertion. This measured angle will be used to compare times of needle visibility dependent to insertion angle of the needle. Significant differences may appear especially in steep angles of needle.

In this study we will use Naropin® (Ropivaciane, 7.5mg/ml) as local anaesthetic for all UGRA.

Not Provided
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Supportive Care
  • Anaesthesia
  • Trauma
Device: ANV(R)

Device: Advanced Needle Visualization Technology ®

Software update for SonoSites M-Turbo® and S-series™ ultrasound systems with enhanced 15-20Mhz ultrasound probe.

Arms: ANV ® Group

Other Name: SonoSite M-Turbo Mbe
  • No Intervention: Standard Treatment Group
    Patients receiving ultrasound guided regional anaesthesia without using Advanced Needle Visualization Technology(R)
  • Active Comparator: ANV ® Group
    Patients receiving ultrasound guided regional anaesthesia with using Advanced Needle Visualization Technology(R)
    Intervention: Device: ANV(R)

*   Includes publications given by the data provider as well as publications identified by Identifier (NCT Number) in Medline.
Unknown status
May 2012
May 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients, who give consent and undergo a femoral or supraclavicular nerve block.

Exclusion Criteria:

  • Patients get excluded if they refused or are unable to give consent by other reasons
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Contact information is only displayed when the study is recruiting subjects
Not Provided
Not Provided
Reinhard Hahn, Medical University of Vienna
Medical University of Vienna
Not Provided
Principal Investigator: Reinhard Hahn, Univ. Lektor Dr. Medical University of Vienna
Medical University of Vienna
April 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP