Catheter Over Needle vs Catheter Through Needle

Sponsor
Sir Charles Gairdner Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02431858
Collaborator
(none)
110
1
2
9.1
12.1

Study Details

Study Description

Brief Summary

To randomize 108 patients undergoing knee replacement surgery to catheter through needle or catheter over needle femoral nerve blocks, then monitor the catheters for leakage to see if there is a difference.

Condition or Disease Intervention/Treatment Phase
  • Device: E-Catheter (Pajunk)
  • Device: Sonolong Catheter (Pajunk)
Phase 4

Detailed Description

Background: Total Knee Replacement Surgery is a commonly performed procedure that causes significant post-operative pain. Continuous femoral nerve blocks are widely used for analgesia as part of a multimodal analgesic regimen for this surgery. They provide sustained analgesia which allows early physiotherapy for rehabilitation. Currently the most common technique for inserting catheters for continuous femoral nerve blocks is to feed a catheter though a needle (CTN) which has been placed close by the nerve. There is a significant rate of leak and dislodgement of these catheters which can lead secondary failure where the catheter is no longer providing analgesia by blocking the nerve (primary failure occurs when the nerve block catheter fails to provide any analgesia from the start). The system to be investigated has a catheter over the needle (CON) which is left in place after the needle is withdrawn. The proposed benefit of this is that there will be a reduction in leak rates and dislodgement. This is because using a CON technique means that the biggest hole will be the diameter of the catheter, rather than CTN where the biggest hole will be the diameter of the needle therefore allowing leak around the outside of the catheter.

Objectives: To ascertain whether or not the catheter over needle technique is superior to catheter through needle technique in terms of a leak rate.

Trial plan: To recruit 108 patients who are having total knee replacement surgery into the study and randomise them into having either CON or CTN continuous femoral nerve blocks.

Study Design

Study Type:
Interventional
Actual Enrollment :
110 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Catheter Over Needle Technique Causes Less Leakage and Secondary Failure Than Catheter Through Needle Technique for Continuous Femoral Nerve Block
Study Start Date :
May 1, 2015
Actual Primary Completion Date :
Feb 1, 2016
Actual Study Completion Date :
Feb 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Catheter Over Needle

The femoral nerve catheter used will be the "E-Catheter" (Pajunk) device which is a novel catheter over needle system.

Device: E-Catheter (Pajunk)
Other Names:
  • Australian Therapeutic Goods Registry (ATGR) no: 133630
  • Active Comparator: Catheter through needle

    The femoral nerve catheter used will be the "Sonolong" catheter (Pajunk) which is a traditional catheter through needle system.

    Device: Sonolong Catheter (Pajunk)
    Other Names:
  • Australian Therapeutic Goods Registry (ATGR) no: 133630
  • Outcome Measures

    Primary Outcome Measures

    1. Catheter leakage [2 days post insertion]

      Any leakage around the catheter insertion site as assessed by visual inspection.

    Secondary Outcome Measures

    1. Overall rate of secondary failure as assessed by the acute pain service on days 1 and 2 post op. [2 days]

      Secondary failure is when a nerve catheter that was previously working has ceased to provide analgesia.

    2. Ease of insertion assessed by the inserting anaesthetist on a 5 point Likert scale. [intraoperative]

      Assess the anaesthetist's opinion on the ease of insertion of the different catheters

    3. Needle visibility assessed by the inserting anaesthetist on a 5 point Likert scale. [intraoperative]

      Assessing the needle visibility in the two different catheter systems.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients presenting to Sir Charles Gairdner Hospital for elective, unilateral, primary total knee replacement.

    • Body mass index 18-40 kg/m2

    • American Society of Anaesthetists (ASA) grade I-III

    Exclusion Criteria:
    • Allergy to local anaesthetic

    • Inability to cooperate

    • Inability to read, speak and understand English

    • Less than 18 years old

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sir Charles Gairdner Hospital Nedlands Western Australia Australia 6009

    Sponsors and Collaborators

    • Sir Charles Gairdner Hospital

    Investigators

    • Principal Investigator: Richard M Edwards, MBBS, Sir Charles Gairdner Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Richard Edwards, Principle Investigator, Sir Charles Gairdner Hospital
    ClinicalTrials.gov Identifier:
    NCT02431858
    Other Study ID Numbers:
    • 2015-011
    First Posted:
    May 1, 2015
    Last Update Posted:
    Apr 19, 2016
    Last Verified:
    Apr 1, 2016
    Keywords provided by Richard Edwards, Principle Investigator, Sir Charles Gairdner Hospital

    Study Results

    No Results Posted as of Apr 19, 2016