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Suprasacral Parallel Shift - Ultrasound/MR Image Fusion Guided Lumbosacral Plexus Block

Primary Purpose

Hip Fractures, Anesthesia Local, Pain, Perioperative

Status
Completed
Phase
Phase 1
Locations
Denmark
Study Type
Interventional
Intervention
Lidocaine-epinephrine added gadoterate meglumine
Sponsored by
Thomas F. Bendtsen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hip Fractures focused on measuring Hip surgery anesthesia, Perioperative analgesia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age ≥ 18 years
  • Volunteers who has given their written and oral informed consent to participate in the study after having fully understood the content and the limitations of the protocol.
  • Normal healthy person (American Society of Anesthesiology [ASA] Classification I)

Exclusion Criteria:

  • Volunteers not able to cooperate in the study
  • Volunteers not able to understand or speak Danish
  • Daily use of analgesics
  • Allergy against the medicines used in the study
  • Drug abuse (according to the investigator's judgement)
  • Alcohol consumption greater than the recommendations of the Danish National Board of Health
  • Contraindication for MRI including pregnancy
  • Volunteer in whom nerve blocks are not possible due to technical reasons
  • Volunteer who are incompetent (ie. surrogate consent is not accepted)

Sites / Locations

  • Department of Anesthesiology and Intensive Care, Aarhus University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Suprasacral Parallel Shift guided by US/MR image fusion

Suprasacral Parallel Shift guided by US

Arm Description

Use of ultrasound/MR image fusion guided Suprasacral Parallel Shift technique to place a lumbar plexus block (20 mL 2% lidocaine with epinephrine added gadoterate meglumine).

Use of ultrasound guided Suprasacral Parallel Shift technique to place a lumbar plexus block (20 mL 2% lidocaine with epinephrine added gadoterate meglumine).

Outcomes

Primary Outcome Measures

Block success
Block success of the clinical relevant lumbosacral nerves that innervate the hip joint capsule estimated as significant motor block of the obturator nerve, the femoral nerve, and the lumbosacral trunk. Motor block is a significant proxy marker of sensory block. Motor block (muscle strength, mmHg) is assessed with a handheld dynamometer.

Secondary Outcome Measures

Plasma lidocaine
Time for preparation
Time for preparation in seconds is defined as the time of placement of the volunteer on the bed until the end of pre-ultrasound scanning
Block procedure time
Block procedure time in seconds is defined as the time of the placement of the ultrasound probe on the skin to until the block needle is pulled out after injection of local anesthetics
Injection site
Block needle depth
Discomfort
Estimated on numeric rating scale 0-10
Mean arterial pressure change
Sensory (cold, warm, touch, pain) block of the dermatomes T12-S3 and the lateral femoral cutaneous nerve
Perineural spread of local anesthetics added gadoterate meglumine
Epidural spread of local anesthetics added gadoterate meglumine
Cost-effectiveness (ICER)
ICER is estimated as the difference in mean marginal cost of the blocks.

Full Information

First Posted
October 28, 2015
Last Updated
February 11, 2016
Sponsor
Thomas F. Bendtsen
Collaborators
AP Moeller Foundation, Aarhus University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02593370
Brief Title
Suprasacral Parallel Shift - Ultrasound/MR Image Fusion Guided Lumbosacral Plexus Block
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
November 2015 (Actual)
Study Completion Date
January 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Thomas F. Bendtsen
Collaborators
AP Moeller Foundation, Aarhus University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The main objective of the trial is to complete a double-blinded randomized controlled trial with crossover design of a lumbosacral plexus block with the Suprasacral Parallel Shift technique guided by ultrasound/magnetic resonance (MR) image fusion vs. Suprasacral Parallel Shift guided by ultrasound by estimating sensory block of the femoral nerve, the obturator nerve, the lumbosacral trunk, and spinal nerve L1 in healthy volunteers.
Detailed Description
The main objective of the trial is to complete a double-blinded randomized controlled trial with crossover design of a one-injection nerve block of the lower part of the lumbar plexus and the upper part of the sacral plexus (Suprasacral Parallel Shift, SSPS) to achieve analgesia of the femoral nerve, the obturator nerve, the lumbosacral trunk, and spinal nerve L1 with SSPS guided by ultrasound/MR image fusion vs. SSPS guided by ultrasound by estimating sensory block of in healthy volunteers by estimating the sensory block of dermatomes of the terminal nerves in healthy volunteers. The secondary objective is to estimate a) preparation and b) procedure time, c) injection site and d) depth, e) discomfort, f) change in MAP, g) plasma lidocaine pharmacokinetics, h) motor and i) sensory block, j) perineural and k) epidural spread of lidocaine-epinephrine added gadotorate meglumine on MRI, and l) cost-effectiveness of SSPS guided by ultrasound/MR image fusion vs. SSPS guided by ultrasound. The investigators hypothesize that block success is higher for SSPS guided by ultrasound/MR image fusion than for SSPS guided by ultrasound.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fractures, Anesthesia Local, Pain, Perioperative
Keywords
Hip surgery anesthesia, Perioperative analgesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Suprasacral Parallel Shift guided by US/MR image fusion
Arm Type
Experimental
Arm Description
Use of ultrasound/MR image fusion guided Suprasacral Parallel Shift technique to place a lumbar plexus block (20 mL 2% lidocaine with epinephrine added gadoterate meglumine).
Arm Title
Suprasacral Parallel Shift guided by US
Arm Type
Active Comparator
Arm Description
Use of ultrasound guided Suprasacral Parallel Shift technique to place a lumbar plexus block (20 mL 2% lidocaine with epinephrine added gadoterate meglumine).
Intervention Type
Drug
Intervention Name(s)
Lidocaine-epinephrine added gadoterate meglumine
Primary Outcome Measure Information:
Title
Block success
Description
Block success of the clinical relevant lumbosacral nerves that innervate the hip joint capsule estimated as significant motor block of the obturator nerve, the femoral nerve, and the lumbosacral trunk. Motor block is a significant proxy marker of sensory block. Motor block (muscle strength, mmHg) is assessed with a handheld dynamometer.
Time Frame
Estimated 40 min after completed intervention. Presented 10 months after last patient last visit (LVLP).
Secondary Outcome Measure Information:
Title
Plasma lidocaine
Time Frame
Blood samples are withdrawn 0, 5, 10, 20, 40, 60, and 90 minutes after intervention. Presented 10 months after LVLP
Title
Time for preparation
Description
Time for preparation in seconds is defined as the time of placement of the volunteer on the bed until the end of pre-ultrasound scanning
Time Frame
Estimated prior to intervention. Presented 10 months after LVLP
Title
Block procedure time
Description
Block procedure time in seconds is defined as the time of the placement of the ultrasound probe on the skin to until the block needle is pulled out after injection of local anesthetics
Time Frame
Estimated during intervention. Presented 10 months after LVLP
Title
Injection site
Time Frame
Estimated at the end of the intervention. Presented 10 months after LVLP
Title
Block needle depth
Time Frame
Estimated at the end of the intervention. Presented 10 months after LVLP
Title
Discomfort
Description
Estimated on numeric rating scale 0-10
Time Frame
Estimated immediately after the intervention. Presented 10 months after LVLP
Title
Mean arterial pressure change
Time Frame
Mean arterial pressure is measured prior intervention and 5 min after intervention. Presented 10 months after LVLP
Title
Sensory (cold, warm, touch, pain) block of the dermatomes T12-S3 and the lateral femoral cutaneous nerve
Time Frame
Estimated 50 min after intervention. Presented 10 months after LVLP
Title
Perineural spread of local anesthetics added gadoterate meglumine
Time Frame
Estimated on MRI sampled 10-30 minutes after intervention. Presented 10 months after LVLP
Title
Epidural spread of local anesthetics added gadoterate meglumine
Time Frame
Estimated on MRI sampled 10-30 minutes after intervention. Presented 10 months after LVLP
Title
Cost-effectiveness (ICER)
Description
ICER is estimated as the difference in mean marginal cost of the blocks.
Time Frame
Calculated after LVLP. Presented 10 months after the last visit of the last volunteer

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Volunteers who has given their written and oral informed consent to participate in the study after having fully understood the content and the limitations of the protocol. Normal healthy person (American Society of Anesthesiology [ASA] Classification I) Exclusion Criteria: Volunteers not able to cooperate in the study Volunteers not able to understand or speak Danish Daily use of analgesics Allergy against the medicines used in the study Drug abuse (according to the investigator's judgement) Alcohol consumption greater than the recommendations of the Danish National Board of Health Contraindication for MRI including pregnancy Volunteer in whom nerve blocks are not possible due to technical reasons Volunteer who are incompetent (ie. surrogate consent is not accepted)
Facility Information:
Facility Name
Department of Anesthesiology and Intensive Care, Aarhus University Hospital
City
Aarhus C
ZIP/Postal Code
8000
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
28396863
Citation
Strid JM, Pedersen EM, Al-Karradi SN, Bendtsen MA, Bjorn S, Dam M, Daugaard M, Hansen MS, Linnet KD, Borglum J, Soballe K, Bendtsen TF. Real-Time Ultrasound/MRI Fusion for Suprasacral Parallel Shift Approach to Lumbosacral Plexus Blockade and Analysis of Injectate Spread: An Exploratory Randomized Controlled Trial. Biomed Res Int. 2017;2017:1873209. doi: 10.1155/2017/1873209. Epub 2017 Mar 15.
Results Reference
derived

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Suprasacral Parallel Shift - Ultrasound/MR Image Fusion Guided Lumbosacral Plexus Block

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