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Protracted Effect of the Ultrasound-guided Saphenous Block (PEUSB)

Primary Purpose

Arthrosis, Unspecified, Ankle and Foot

Status
Completed
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Bupivacaine-adrenaline
Dexamethasone
Sodium chloride
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Arthrosis, Unspecified, Ankle and Foot

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Elective ankle or hind foot surgery either: (1) total ankle arthroplasty, (2) ankle arthrodesis or (3) subtalar arthrodesis
  • Age ≥ 18
  • American Society of Anaesthesiology Classification I-III
  • Informed consent both orally and in writing after the patient has fully understood the protocol and its limitations.

Exclusion Criteria:

  • Communication problems or dementia
  • Allergies to any medical product used in the study
  • Neuropathy of the sciatic or femoral nerve prior to the operation
  • Morbus Charcot-Marie-Tooth disease, diabetic neuropathy, peripheral vascular disease
  • BMI > 35
  • Pregnancy
  • Daily use of opioids
  • Coagulation disorders
  • Infection at the site of injection or systemic infection

Sites / Locations

  • Department of Anesthesiology, Aarhus University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Bupivacaine-adrenalin + sodium chloride

Bupivacaine-adrenaline + Dexamethasone

Arm Description

Single shot saphenous block: 10 mL of 5 mg/mL bupivacaine with 5 μg/mL adrenalin = 50 mg bupivacain and 50 μg adrenalin 1 mL sodium chloride solution

Single shot saphenous block: 10 mL of 5 mg/mL bupivacaine with 5 μg/mL adrenalin = 50 mg bupivacain and 50 μg adrenalin 1 mL of 4 mg/mL dexamethasone = 4 mg dexamethasone

Outcomes

Primary Outcome Measures

Duration of the saphenous nerve block
The duration is registered as the time until the first dose of morphine is taken, and when the pain score is above 3 and located to the frontal or medial side of the ankle. Morphine is administered intravenously by a patient controlled pump (PCA - Patient Controlled Analgesia)

Secondary Outcome Measures

Cumulated opioid consumption
Registered by the PCA pump
Pain score
NRS (numeric rating scale)
Pain localization
Lateral or medial side of the ankle
Test of sensory block
The sensory block of the peroneal nerve is tested on the dorsal side of the toes and the tibial nerve on the plantar side of the toes. The ankle and lower leg is covered in cast, and therefore the saphenous nerve is tested around the tibial tuberosity because this area is innervated by the infra-patellar nerve, which is a branch of the saphenous nerve

Full Information

First Posted
January 13, 2015
Last Updated
February 11, 2016
Sponsor
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT02346110
Brief Title
Protracted Effect of the Ultrasound-guided Saphenous Block
Acronym
PEUSB
Official Title
Comparison of the Effect of a Single Shot Saphenous Block With Plain Bupivacaine vs. Protracted Bupivacaine Mixture as a Supplement to Continuous Sciatic Catheter After Major Ankle and Foot Surgery
Study Type
Interventional

2. Study Status

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

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study focuses on optimizing the postoperative pain treatment after major foot and ankle surgery by prolonging the duration of the ultrasound-guided saphenous block. The currently used single shot saphenous block only covers half of the pain intensive period from the saphenous territory, which results in a sharp, break-through pain requiring opioids. The hypothesis is that this protracted mixture will keep the patients free of pain without the use of opioids for the entire pain intensive period and thus increase rehabilitation and patients' satisfaction.
Detailed Description
Half of the patients will receive a single shot saphenous block with 10 mL bupivacaine-adrenalin and 1 mL of sodium chloride solution, while the other half will receive 10 mL of bupivacaine-adrenalin and 1 mL of dexamethasone. The block is strictly a sensory block because it is a selective, sub-sartorial saphenous block at mid-thigh level without any anesthetic effect on the femoral nerve. The adjuvant dexamethasone has increasingly become a subject of interest regarding a protracted effect, which has been shown in several studies. However, the precise mechanism of action remains speculative, and the results are contradictory regarding the discussion whether the effect is systemic or local. The effect may stem from decreased nociceptive C-fibre activity via a direct action on glucocorticoid receptors and inhibitory potassium channels. Another suggestion is a vasoconstrictive effect, which reduces the systemic uptake of local anaesthetics or a systemic anti-inflammatory effect. Prolonging the effect of the single shot saphenous block by adding dexamethasone will reduce the need for opioids, which will reduce the risk of adverse effects like nausea, vomiting and respiratory depression. Furthermore, newer studies show that inadequate pain alleviation in the early postoperative period is a risk factor in developing chronic persistent pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Arthrosis, Unspecified, Ankle and Foot

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bupivacaine-adrenalin + sodium chloride
Arm Type
Active Comparator
Arm Description
Single shot saphenous block: 10 mL of 5 mg/mL bupivacaine with 5 μg/mL adrenalin = 50 mg bupivacain and 50 μg adrenalin 1 mL sodium chloride solution
Arm Title
Bupivacaine-adrenaline + Dexamethasone
Arm Type
Experimental
Arm Description
Single shot saphenous block: 10 mL of 5 mg/mL bupivacaine with 5 μg/mL adrenalin = 50 mg bupivacain and 50 μg adrenalin 1 mL of 4 mg/mL dexamethasone = 4 mg dexamethasone
Intervention Type
Drug
Intervention Name(s)
Bupivacaine-adrenaline
Other Intervention Name(s)
Marcain-adrenalin
Intervention Description
50 mg bupivacaine and 50 μg adrenalin
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Other Intervention Name(s)
Dexagalen
Intervention Description
4 mg
Intervention Type
Other
Intervention Name(s)
Sodium chloride
Other Intervention Name(s)
NaCL
Intervention Description
1 mL of sodium chloride solution as placebo
Primary Outcome Measure Information:
Title
Duration of the saphenous nerve block
Description
The duration is registered as the time until the first dose of morphine is taken, and when the pain score is above 3 and located to the frontal or medial side of the ankle. Morphine is administered intravenously by a patient controlled pump (PCA - Patient Controlled Analgesia)
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Cumulated opioid consumption
Description
Registered by the PCA pump
Time Frame
48 hours
Title
Pain score
Description
NRS (numeric rating scale)
Time Frame
Arrival at the Perioperative Section which will be within 30 minutes after surgery. Departure from the Perioperative Section which is expected to be on average 2 hours after surgery. 6, 12, 24, 30, 36, 42 and 48 hours after surgery
Title
Pain localization
Description
Lateral or medial side of the ankle
Time Frame
Arrival at the Perioperative Section which will be within 30 minutes after surgery. Departure from the Perioperative Section which is expected to be on average 2 hours after surgery. 6, 12, 24, 30, 36, 42 and 48 hours after surgery
Title
Test of sensory block
Description
The sensory block of the peroneal nerve is tested on the dorsal side of the toes and the tibial nerve on the plantar side of the toes. The ankle and lower leg is covered in cast, and therefore the saphenous nerve is tested around the tibial tuberosity because this area is innervated by the infra-patellar nerve, which is a branch of the saphenous nerve
Time Frame
Arrival at the Perioperative Section which will be within 30 minutes after surgery. Departure from the Perioperative Section which is expected to be on average 2 hours after surgery. 6, 12, 24, 30, 36, 42 and 48 hours after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Elective ankle or hind foot surgery either: (1) total ankle arthroplasty, (2) ankle arthrodesis or (3) subtalar arthrodesis Age ≥ 18 American Society of Anaesthesiology Classification I-III Informed consent both orally and in writing after the patient has fully understood the protocol and its limitations. Exclusion Criteria: Communication problems or dementia Allergies to any medical product used in the study Neuropathy of the sciatic or femoral nerve prior to the operation Morbus Charcot-Marie-Tooth disease, diabetic neuropathy, peripheral vascular disease BMI > 35 Pregnancy Daily use of opioids Coagulation disorders Infection at the site of injection or systemic infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Fichtner Bendtsen, MD, phD
Organizational Affiliation
Department of Anesthesiology, Aarhus University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Anesthesiology, Aarhus University Hospital
City
Aarhus
State/Province
Midtjylland
ZIP/Postal Code
8000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Protracted Effect of the Ultrasound-guided Saphenous Block

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