- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01527812
Optimal Positioning of Local Anaesthetic in Femoral Nerve Block Prior to Hip Surgery
Optimal Positioning of Local Anaesthetic in Femoral Nerve Block Prior to Operative Fixation of Fractured Neck of Femur
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Fractured neck of femur is a common cause of admission to hospital in elderly patients and requires operative fixation. The recommended anaesthetic technique for these cases is spinal anaesthesia, which is performed with the patient in lateral decubitus. Positioning the patient prior to administering spinal anaesthesia is the most painful manouvre due to the movement of the fractured bone.
Regional anaesthesia is effective in alleviating pain due to trauma, and it has the advantage of producing localized but complete pain relief (1). Femoral nerve blockade prior to positioning for spinal anaesthesia provides excellent pain relief and is a well tolerated procedure (2-5).
Using ultrasound guided femoral nerve block is a relative new method to improving the block success rate. It is widely used in our hospital. In a recent study Casati and al. showed a 42 % decrease of ED50% using ultrasound for localization of the femoral nerve (6). In a recent editorial by Brian D. Sites was mentioned that the positioning of the local anaesthetic in ultrasound guided blocks is unclear (7). We currently follow different patterns in relation to injection of the local anaesthetic solution around the femoral nerve. One of them is a circumferencial spread around the nerve. This, however, needs several needle passes which are likely to be painful for the patient. Another option is injecting the local anaesthetic on one side, above or below the nerve without changing the position of the tip of the needle, avoiding patient discomfort. Whether this results in a comparable quality of sensory block is unknown. The femoral nerve is separated in branches at this level and we assume that the spread of local anaesthetic may influence the quality and the distribution of the block. We propose to study the characteristics of femoral nerve block in relation to different patterns of local anaesthetic injection (circumferencial, inferior or superior).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Cork, Ireland
- Cork University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Fractured neck of femur surgical fixation performed under spinal anaesthesia
- ASA I to III
Exclusion Criteria:
- Patient refusal
- Coagulation disorders
- Head injury or other associated injuries
- Previous vascular surgery in the femoral area.
- Loss of consciousness and signs of acute coronary syndrome
- Mini-Mental Score < 25 (see appendix 3)
- Allergy to lignocaine,
- Skin lesions/infection at site of injection
- Sepsis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Above the femoral nerve
In Group I we will inject the local anaesthetic below the fascia iliaca and above the femoral nerve.
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We will perform an ultrasound guided femoral nerve block.
For locating the nerve a 5 cm, 6-13 MHz linear probe (Sonosite Turbo M, Bothwell WA, USA) will be used.
After the examination of the anatomy of the femoral artery we will fix the probe transversal to the thigh below the inguinal crease and above the ramification of deep femoral artery and make skin marks on this position.
A 22 G 50 mm long Stimuplex BBraun needle will be used.
15 ml 2 % lignocaine will be injected.
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Experimental: Below the femoral nerve
In Group II we will inject the local anaesthetic below the femoral nerve and above the fascia of the iliopsoas muscle.
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We will perform an ultrasound guided femoral nerve block.
For locating the nerve a 5 cm, 6-13 MHz linear probe (Sonosite Turbo M, Bothwell WA, USA) will be used.
After the examination of the anatomy of the femoral artery we will fix the probe transversal to the thigh below the inguinal crease and above the ramification of deep femoral artery and make skin marks on this position.
A 22 G 50 mm long Stimuplex BBraun needle will be used.
15 ml 2 % lignocaine will be injected.
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Experimental: Circumferential
In Group III a circumferential spread will be achieved with multiple injections.
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We will perform an ultrasound guided femoral nerve block.
For locating the nerve a 5 cm, 6-13 MHz linear probe (Sonosite Turbo M, Bothwell WA, USA) will be used.
After the examination of the anatomy of the femoral artery we will fix the probe transversal to the thigh below the inguinal crease and above the ramification of deep femoral artery and make skin marks on this position.
A 22 G 50 mm long Stimuplex BBraun needle will be used.
15 ml 2 % lignocaine will be injected.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Verbal rating scale (VRS) pain scores after positioning the patient to performing the spinal anaesthesia.
Time Frame: The patient will be assessed in every five minutes up to 30 minutes after the femoral nerve block.
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Independent blinded observer will assess the patient in the first 30 minutes, in every 5 minute. Sensory perception will be assess by using cold spray in the area of the terminal branch of femoral nerve. We will assess the pain on passive movement of the limb (elevating 30 degree) using verbal rating scale (VRS) pain score 1-10. When the patient reports less than 4 at the VRS the patient will be positioned for spinal anaesthesia. If the threshold isn't achieved by 30 minutes, the block will be classified as failure. Additional opioid medication and/or sedation will be administered. |
The patient will be assessed in every five minutes up to 30 minutes after the femoral nerve block.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Sensory distribution of the nerve block.
Time Frame: The patient will be assessed in every five minutes up to 30 minutes after the femoral nerve block.
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An independent blinded observer (not present during block placement) will assess in the first 30 minutes (at 5 minute intervales) the sensory nerve block using a modified Bromage score.
Sensory perception will be assessed using cold (ethyl chloride spray) in the area of the vastus medialis, vastus intermedius, vastus lateralis and saphenous nerve innervation area (terminal branch of femoral nerve).
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The patient will be assessed in every five minutes up to 30 minutes after the femoral nerve block.
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Number of needle passes
Time Frame: during performing the femoral nerve block
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The Anaesthestist who performing the femoral nerve block was asked how many needle passes needed for the femoral nerve block.
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during performing the femoral nerve block
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Femoral nerve block onset time
Time Frame: In the first 30 minutes after the femoral nerve block
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We will assess the pain on passive movement of the limb (elevating 30 degree from the initial positioning) using verbal rating scale (VRS) pain score 1-10.
When the patient reports less than 4 at the VRS the sensory block will be deemed adequate and the patient will be positioned on the side for spinal anaesthesia.
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In the first 30 minutes after the femoral nerve block
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Patient satisfaction
Time Frame: After the surgery in the recovery area before the patient will be discharged to the ward.
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After the surgery during the recovery time, we will ask the patients regarding there Satisfaction, will be used visual analog scale 0-100 mm for measurement.
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After the surgery in the recovery area before the patient will be discharged to the ward.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Szilard Szucs, MD, Cork University Hospital, Ireland
Publications and helpful links
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- ECM 4 (zz) 08/12/09 (Other Identifier: Clinical Research Ethics Committee of the Cork Teaching Hospitals)
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Clinical Trials on Fractured Neck of Femur
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Cork University HospitalUniversity of BristolUnknown
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Royal Berkshire NHS Foundation TrustDePuy InternationalSuspendedFractured Neck of FemurUnited Kingdom
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Brno University HospitalSt. Anne's University Hospital Brno, Czech RepublicCompletedFracture of Neck of Femur (Hip)Czech Republic
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