Randomized Controlled Trial for Ankle Fracture Pain Control
Primary Purpose
Ankle Fractures
Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Long-Acting Local Anesthesia
Regional Anesthesia
Sponsored by
About this trial
This is an interventional treatment trial for Ankle Fractures
Eligibility Criteria
Inclusion Criteria:
- Sustained a bimalleolar ankle fracture (OTA/AO type 44 A2, B2, C1, and C2 fracture) with surgery indicated and an approach with medial and lateral incisions planned Syndesmotic injuries will be included, due to the practical difficulty of reliably determining the presence of a syndesmotic injury preoperatively Trimalleolar ankle fractures where fixation of the posterior malleolus is not planned will also be included
- Isolated Injury
Exclusion Criteria:
- Unifocal malleolar fractures
- Bimalleolar fractures where fixation of only one malleolus is planned
- Posterior malleolus fractures requiring fixation
- Patients ineligible for a peripheral nerve block (e.g. concern for compartment syndrome)
- Open injury
- Patients treated with external fixation
- Neurologic condition that would confound results (e.g. peripheral neuropathy)
- Inability to consent
- Chronic opioid use
- History of opiate abuse
- Polytrauma as defined as additional boney injury, visceral injury or moderate soft tissue injury (requiring suture repair or other invasive procedure)
- Prisoners (unlikely to be accessible for follow-up)
- Pregnant patients
- Non-English-speaking subjects (post-operative data collection procedure involves conversations via phone calls. As we do not have access to translators for this research project, we will work exclusively with English-speaking subjects).
- Subjects unable to take the standard post-operative pain regimen that consists of gabapentin, oxycodone, acetaminophen, and ibuprofen.
Sites / Locations
- Lahey Hospital & Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Experimental
Experimental
Arm Label
Traditional Pain Control Care
Regional Anesthesia
Long-Acting Local Anesthesia
Arm Description
Standard of care post-operative pain control with oral narcotics
Single injection perioperative peripheral nerve block + followed by administration of oral narcotics on a need-based system
Subcutaneous local cocktail injection + followed by administration of oral narcotics on a need-based system
Outcomes
Primary Outcome Measures
Oral Narcotics / Morphine Milligram Equivalents (MME) given
The medical record (EPIC) will be used to determine the total morphine equivalents given to the patient post-surgery, including recovery unit administration of narcotics in the immediate post-operative period.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03696199
Brief Title
Randomized Controlled Trial for Ankle Fracture Pain Control
Official Title
A Prospective, Randomized Trial Evaluating Regional Anesthesia, Long-Acting Local Anesthesia, and Traditional Care for Pain Control of Operatively Treated Ankle Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2020 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
September 1, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Lahey Clinic
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
This project is a multicenter, three armed, prospective randomized control trial studying the effectiveness of a long-acting local anesthetic "cocktail" in patients undergoing operative fixation of ankle fractures.
Detailed Description
This study is a multicenter, three armed, prospective randomized control trial studying the effect of a long-acting local anesthetic "cocktail" in patients undergoing operative fixation of ankle fractures.
Primary Hypothesis Driven Aims:
Determine the effectiveness of a local anesthesia "cocktail" compared to regional block or standard of care in controlling pain in operatively treated ankle fractures. Nearly one out of ten fractures treated by both orthopaedic traumatologists and general orthopaedic surgeons taking call are ankle fractures. As such, effective pain control in this group of patients represents an opportunity to make a large impact, especially in the context of the current opioid epidemic. Improved pain control can help improve patient satisfaction, outcomes, decrease length of stay, cost of care, and complications associated with traditional narcotic use.
Hypothesis 1A: Patients receiving the intraoperative cocktail will have improved post-operative pain control compared to those receiving a peri-operative nerve block or standard of care.
Hypothesis 1B: Patients receiving the intraoperative cocktail or peri-operative nerve block will have improved post-operative pain control when compared to standard of care.
Null Hypothesis 1: There will be no difference in post-operative pain control between all treatment arms.
Determine the economic impact of cocktail and regional blocks in ankle fractures. A common concern with the use of regional blocks is the cost of the additional procedure, along with logistic delays which are associated with coordinating a separate procedure. This study would provide valuable data about the additional costs associated with regional blocks and with cocktail administration which could help aid in making economically conscious treatment decisions.
Hypothesis 2: Local cocktail administration will have significantly lower costs than regional block, and not be significantly more expensive than standard of care.
Null Hypothesis 2: There is no difference in cost between the modalities.
Secondary Aim:
Demonstrate the use of long-acting local anesthetic as a viable pain management strategy in fracture surgery. Although long-acting local anesthetics have an established track record in arthroplasty, there is a paucity of evidence guiding their use in fractures. Small case series in trauma and foot/ankle patients have been encouraging, but a rigorously conducted, prospective trial in a relatively homogeneous group could generate pilot data to validate the use of long acting local anesthetics in fracture surgery. This knowledge may be translatable to other extremity injuries as well, having a greater impact than the scope of the proposed trial.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Fractures
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Traditional Pain Control Care
Arm Type
No Intervention
Arm Description
Standard of care post-operative pain control with oral narcotics
Arm Title
Regional Anesthesia
Arm Type
Experimental
Arm Description
Single injection perioperative peripheral nerve block + followed by administration of oral narcotics on a need-based system
Arm Title
Long-Acting Local Anesthesia
Arm Type
Experimental
Arm Description
Subcutaneous local cocktail injection + followed by administration of oral narcotics on a need-based system
Intervention Type
Drug
Intervention Name(s)
Long-Acting Local Anesthesia
Other Intervention Name(s)
Local Cocktail
Intervention Description
The cocktail consists of:
0.5% Ropivicaine, 24.6 mL
Clonidine 100 mcg/mL, 0.4mL
Epinephrine 1mg/mL, 0.5mL
Saline to total volume of 50 mL (24.5mL of saline)
The total amount of solution prepared is 50mL, but typically 30mL is used based on the size of the incision. The total volume administered will be recorded.
Intervention Type
Drug
Intervention Name(s)
Regional Anesthesia
Other Intervention Name(s)
Ropivicaine
Intervention Description
0.5% ropivicaine - 30mL each sciatic and femoral/saphenous nerve, ultrasound guided
Primary Outcome Measure Information:
Title
Oral Narcotics / Morphine Milligram Equivalents (MME) given
Description
The medical record (EPIC) will be used to determine the total morphine equivalents given to the patient post-surgery, including recovery unit administration of narcotics in the immediate post-operative period.
Time Frame
72 postoperative hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sustained a bimalleolar ankle fracture (OTA/AO type 44 A2, B2, C1, and C2 fracture) with surgery indicated and an approach with medial and lateral incisions planned Syndesmotic injuries will be included, due to the practical difficulty of reliably determining the presence of a syndesmotic injury preoperatively Trimalleolar ankle fractures where fixation of the posterior malleolus is not planned will also be included
Isolated Injury
Exclusion Criteria:
Unifocal malleolar fractures
Bimalleolar fractures where fixation of only one malleolus is planned
Posterior malleolus fractures requiring fixation
Patients ineligible for a peripheral nerve block (e.g. concern for compartment syndrome)
Open injury
Patients treated with external fixation
Neurologic condition that would confound results (e.g. peripheral neuropathy)
Inability to consent
Chronic opioid use
History of opiate abuse
Polytrauma as defined as additional boney injury, visceral injury or moderate soft tissue injury (requiring suture repair or other invasive procedure)
Prisoners (unlikely to be accessible for follow-up)
Pregnant patients
Non-English-speaking subjects (post-operative data collection procedure involves conversations via phone calls. As we do not have access to translators for this research project, we will work exclusively with English-speaking subjects).
Subjects unable to take the standard post-operative pain regimen that consists of gabapentin, oxycodone, acetaminophen, and ibuprofen.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eric Swart, MD
Phone
781-744-2629
Email
eric.f.swart@lahey.org
First Name & Middle Initial & Last Name or Official Title & Degree
John Garfi, MS
Phone
781-744-2629
Email
john.garfi@lahey.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric Swart, MD
Organizational Affiliation
Lahey Hospital & Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lahey Hospital & Medical Center
City
Burlington
State/Province
Massachusetts
ZIP/Postal Code
01805
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric Swart, MD
Phone
781-744-2629
12. IPD Sharing Statement
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Randomized Controlled Trial for Ankle Fracture Pain Control
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