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Radiofrequency Ablation: Treatment for Posterior Element Pain From Vertebral Compression Fractures

Primary Purpose

Vertebral Compression Fracture, Facet Joint Pain

Status
Suspended
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Radiofrequency ablation of the medial branch nerves
Non-steroidal anti-inflammatory drugs
Bisphosphonates
Acetaminophen
Physical therapy
Opioids
Sponsored by
University of California, Davis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vertebral Compression Fracture

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

I• Inclusion

  • 18-90 years old
  • Male or female
  • Age of fracture greater than or equal to 6 weeks
  • Single Level Vertebral Compression Fracture
  • Vertebral compression fracture Thoraic-9 to Lumbar-5
  • NRS >6/10

    • Exclusion

  • <18 or >90 yo
  • Uncorrectable Coagulopathy
  • Multiple Level Vertebral Compression Fractures
  • Surgery within 60 days of presentation
  • Active infection
  • Rhuematologic disease
  • Significant neurologic deficit
  • Radicular pain
  • Chronic low back pain in last year
  • Inability to give consent
  • Cognitive impairment
  • Patients with Ongoing Litigation or Worker's Compensation Cases

Sites / Locations

  • UC Davis Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Control Group

Treatment Group

Crossover Group

Arm Description

The control group will receive usual care for treatment of vertebral compression fractures, which will consist of but not limited to: physical therapy, opioids, NSAIDs, acetaminophen and bisphosphonates as indicated. They will have the option of crossing over (see "Crossover Group") at twelve weeks.

The treatment group will receive usual care for treatment and the treatment procedure comprised of the Medial Branch Block and Radiofrequency Ablation. In cases where a medial branch nerve block has confirmed there is pain relief, a radiofrequency ablation is considered. These patients will continue their usual care therapy as well.

This group will comprise of patients within the control group who after 12 weeks of usual therapy will have the option of crossing over to the treatment group. Once crossed over, their treatment and course and measurements will be identical to that of the treatment group.

Outcomes

Primary Outcome Measures

Change in Visual Analog Scale (VAS) of subjective pain at dedicated Time Frames listed below.
VAS pain scale (0-10 scale): Overall, at rest, and in bed at night The VAS Pain scale is a measure of pain intensity. For pain intensity, the scale is anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 10). Subjects will report their pain prior to the procedure and at dedicated intervals after to assess change in pain intensity they experience.

Secondary Outcome Measures

Roland-Morris Disability Questionnaire at dedicated time frames listed below to assess change.
The Roland-Morris Questionnaire (RMQ) is a self-administered disability measure in which greater levels of disability are reflected by higher numbers on a 24-point scale. The RMQ has been shown to yield reliable measurements, which are valid for inferring the level of disability, and to be sensitive to change over time for groups of patients with low back pain. It is a series of 24 questions in which a "Yes" response appoints one point. A total score of is 24 possible. Clinical improvement over time can be graded based on the analysis of serial questionnaire scores. If, for example, at the beginningof treatment, a patient's score was 12 and, at the conclusion of treatment, her score was 2 (10 points of improvement), we would calculate an 83% (10/12 x 100) improvement.
QUALEFFO-41 (Quality of Life questionnaire) Scale at dedicated time frames listed below to assess change.
The Qualeffo-41 is a specific quality of life instrument, which is developed for patients with vertebral compression fractures. This questionnaire comprised of 41 questions, covers main aspects of quality of life: pain, physical functions, social functions, general health and mental health. All answers are standardized so that 1 represents the best and 5 (or 3, or 4) represents the worst quality of life (reverse scores on questions 33, 34, 35, 37, 39, 40). The total score is calculated by summing all answers of questions 1-41. The raw total score ranges from 41 to 205 (or less when some answers are missing) and this is transformed to scores from 0 to 100. The higher the score the poorer the quality of life.
Patient Health Questionnaire (PHQ-9) at dedicated Time Frames listed below.
The PHQ-9 is a multipurpose instrument for monitoring and measuring the severity of depression. The PHQ-9 incorporates leading major depressive symptoms into a brief self-report tool. It is comprised of a series of 9 questions that assess a series of feelings/symptoms related to clinical depression over the past two weeks and are graded on a scale of 0-3 (gradation of not at all 0 to every day 3). The scores are tallied up for a total score of 0 to 27. The higher the score the greater the severity of the depression.

Full Information

First Posted
August 14, 2018
Last Updated
December 16, 2022
Sponsor
University of California, Davis
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1. Study Identification

Unique Protocol Identification Number
NCT03651804
Brief Title
Radiofrequency Ablation: Treatment for Posterior Element Pain From Vertebral Compression Fractures
Official Title
Radiofrequency Ablation of the Medial Branch Nerve as a Novel Treatment for Posterior Element Pain From Vertebral Compression Fractures
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Suspended
Why Stopped
Difficulty recruiting members
Study Start Date
April 10, 2019 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
June 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis

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.
No

5. Study Description

Brief Summary
The purpose of this study is to test the efficacy of radiofrequency ablation of the medial branch nerves (RFA-MBN) in relieving pain and improving physical function in patients with subacute and chronic vertebral compression fractures (VCF).
Detailed Description
The study examines a novel approach to treat pain associated with VCFs. The usual care therapy currently involves utilizing physical therapy, non-steroidal anti-inflammatory medications, opioids, and bone re-building medications known as bisphosphonates. A usual treatment plan may include some, if not all the above. There is growing evidence that the posterior spinal elements contribute to pain that patients with VCFs experience. RFA-MBN, which targets these posterior spinal elements, may provide more sustained pain relief and improved physical function compared to usual care for these fractures. The procedure essentially "ablates with heat" the medial branch nerves which send pain signals from the posterior elements to the brain. Patients will be randomly selected into one of two groups. The treatment group will receive the RFA-MBN procedure along with usual care therapy. The control group will undergo usual care. The control group will have the option to cross over to receive RFA-MBN at a defined interval during the study. There will be follow up visits at various intervals to compare pain relief and function based on various surveys of the treatment, control, and cross-over groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vertebral Compression Fracture, Facet Joint Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
Active Comparator
Arm Description
The control group will receive usual care for treatment of vertebral compression fractures, which will consist of but not limited to: physical therapy, opioids, NSAIDs, acetaminophen and bisphosphonates as indicated. They will have the option of crossing over (see "Crossover Group") at twelve weeks.
Arm Title
Treatment Group
Arm Type
Active Comparator
Arm Description
The treatment group will receive usual care for treatment and the treatment procedure comprised of the Medial Branch Block and Radiofrequency Ablation. In cases where a medial branch nerve block has confirmed there is pain relief, a radiofrequency ablation is considered. These patients will continue their usual care therapy as well.
Arm Title
Crossover Group
Arm Type
Active Comparator
Arm Description
This group will comprise of patients within the control group who after 12 weeks of usual therapy will have the option of crossing over to the treatment group. Once crossed over, their treatment and course and measurements will be identical to that of the treatment group.
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency ablation of the medial branch nerves
Other Intervention Name(s)
RFA-MBB
Intervention Description
A radiofrequency ablation (RFA) is a procedure in which a heat lesion via a needle is created on the nerve that transmits the pain signal in order to interrupt the brain to interrupt the painful signal to the brain. We will target the medial branch nerves.
Intervention Type
Drug
Intervention Name(s)
Non-steroidal anti-inflammatory drugs
Other Intervention Name(s)
NSAID
Intervention Description
Some of the most commonly used pain medicines in adults. NSAIDs block proteins, called enzymes, in the body that play a role in pain and inflammation. They include aspirin, ibuprofen (Advil, Motrin), naproxen (Aleve), and many other generic and brand name drugs.
Intervention Type
Drug
Intervention Name(s)
Bisphosphonates
Intervention Description
A class of drugs that prevent the loss of bone density and are used to treat osteoporosis and similar diseases.
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Other Intervention Name(s)
Tylenol
Intervention Description
A medicine used to treat pain and fever. It is typically used for mild to moderate pain relief. Commonly known as Tylenol.
Intervention Type
Behavioral
Intervention Name(s)
Physical therapy
Intervention Description
Physical Therapy.
Intervention Type
Drug
Intervention Name(s)
Opioids
Intervention Description
Opioids are narcotics that act on opioid receptors to produce morphine-like effects and medically they are primarily used for pain relief.
Primary Outcome Measure Information:
Title
Change in Visual Analog Scale (VAS) of subjective pain at dedicated Time Frames listed below.
Description
VAS pain scale (0-10 scale): Overall, at rest, and in bed at night The VAS Pain scale is a measure of pain intensity. For pain intensity, the scale is anchored by "no pain" (score of 0) and "pain as bad as it could be" or "worst imaginable pain" (score of 10). Subjects will report their pain prior to the procedure and at dedicated intervals after to assess change in pain intensity they experience.
Time Frame
0 weeks, 1 week, 12 weeks, 6 months
Secondary Outcome Measure Information:
Title
Roland-Morris Disability Questionnaire at dedicated time frames listed below to assess change.
Description
The Roland-Morris Questionnaire (RMQ) is a self-administered disability measure in which greater levels of disability are reflected by higher numbers on a 24-point scale. The RMQ has been shown to yield reliable measurements, which are valid for inferring the level of disability, and to be sensitive to change over time for groups of patients with low back pain. It is a series of 24 questions in which a "Yes" response appoints one point. A total score of is 24 possible. Clinical improvement over time can be graded based on the analysis of serial questionnaire scores. If, for example, at the beginningof treatment, a patient's score was 12 and, at the conclusion of treatment, her score was 2 (10 points of improvement), we would calculate an 83% (10/12 x 100) improvement.
Time Frame
0 weeks, 1 week, 12 weeks, 6 months
Title
QUALEFFO-41 (Quality of Life questionnaire) Scale at dedicated time frames listed below to assess change.
Description
The Qualeffo-41 is a specific quality of life instrument, which is developed for patients with vertebral compression fractures. This questionnaire comprised of 41 questions, covers main aspects of quality of life: pain, physical functions, social functions, general health and mental health. All answers are standardized so that 1 represents the best and 5 (or 3, or 4) represents the worst quality of life (reverse scores on questions 33, 34, 35, 37, 39, 40). The total score is calculated by summing all answers of questions 1-41. The raw total score ranges from 41 to 205 (or less when some answers are missing) and this is transformed to scores from 0 to 100. The higher the score the poorer the quality of life.
Time Frame
0 weeks, 1 week, 12 weeks, 6 months
Title
Patient Health Questionnaire (PHQ-9) at dedicated Time Frames listed below.
Description
The PHQ-9 is a multipurpose instrument for monitoring and measuring the severity of depression. The PHQ-9 incorporates leading major depressive symptoms into a brief self-report tool. It is comprised of a series of 9 questions that assess a series of feelings/symptoms related to clinical depression over the past two weeks and are graded on a scale of 0-3 (gradation of not at all 0 to every day 3). The scores are tallied up for a total score of 0 to 27. The higher the score the greater the severity of the depression.
Time Frame
0 weeks, 1 week, 12 weeks, 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
I• Inclusion 18-90 years old Male or female Age of fracture greater than or equal to 6 weeks Single Level Vertebral Compression Fracture Vertebral compression fracture Thoraic-9 to Lumbar-5 NRS >6/10 • Exclusion <18 or >90 yo Uncorrectable Coagulopathy Multiple Level Vertebral Compression Fractures Surgery within 60 days of presentation Active infection Rhuematologic disease Significant neurologic deficit Radicular pain Chronic low back pain in last year Inability to give consent Cognitive impairment Patients with Ongoing Litigation or Worker's Compensation Cases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David Copenhaver, MD
Organizational Affiliation
UC Davis Medical Center, Department of Anesthesiology and Pain Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Davis Medical Center
City
Davis
State/Province
California
ZIP/Postal Code
95817
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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21337428
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Links:
URL
https://studypages.com/s/radiofrequency-ablation-heat-therapy-to-reduce-nerve-pain-for-vertebral-compression-fracture-pain-402785/
Description
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Radiofrequency Ablation: Treatment for Posterior Element Pain From Vertebral Compression Fractures

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