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Cooled Radiofrequency Ablation vs. Thermal Radiofrequency Ablation

Primary Purpose

Chronic Thoracic Back Pain

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
c-RFA
tRFA
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Thoracic Back Pain

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 or older
  • Chronic thoracic spine mediated back pain of 3 months duration or longer
  • Absence of focal neurologic signs or symptoms related to thoracic radiculopathy
  • Failure to respond to conservative measures in the form of oral medication and physical therapy
  • More than 50% reduction in their pain less than 2 months duration following a series of 2 diagnostic thoracic medial branch blocks of the affected joints using 1 ml of 1% lidocaine in the first procedure and bupivacaine 0.5 % in the second time

Exclusion Criteria:

  • Untreated coagulopathy
  • Concomitant medical (e.g. uncontrolled cardiac condition) or psychiatric illness (e.g., untreated depression) likely to endanger the patient or compromise treatment outcomes
  • Pregnancy
  • Malignancy
  • Systemic or local infection

Sites / Locations

  • Cleveland Clinic

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

c-RFA

t-RFA

Arm Description

cooled radiofrequency ablation

thermal radiofrequency ablation

Outcomes

Primary Outcome Measures

Pain Score on the visual analogue scale

Secondary Outcome Measures

Full Information

First Posted
February 21, 2014
Last Updated
February 22, 2023
Sponsor
The Cleveland Clinic
Collaborators
Kimberly-Clark Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT02073292
Brief Title
Cooled Radiofrequency Ablation vs. Thermal Radiofrequency Ablation
Official Title
A Randomized Controlled Trial Comparing Thermal and Cooled Radiofrequency Ablation Techniques of Thoracic Facets' Medial Branches to Manage Thoracic Pain
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
March 2014 (Actual)
Primary Completion Date
December 15, 2022 (Actual)
Study Completion Date
December 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Cleveland Clinic
Collaborators
Kimberly-Clark Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Nerves in your body transmit signals to and from your brain and the cells in your body. In the event of an injury or disease, these nerves transmit pain. Sometimes, when an injury doesn't heal, chronic pain can develop. One way to treat chronic pain is to interrupt these pain signals. One method of doing this is to use Radio frequency ablation (RFA). Radio frequency ablation (RFA) is a medical procedure in which heat is generated from high frequency electrical current in order to lesion (burn) nervous tissue. Radiofrequency ablation is used to treat many conditions in several areas of the body including cardiac (heart) as well as chronic pain. Probes (needles) are inserted into the body to a specific location and the electrical current is passed through these needles. This electrical current creates heat in your body and forms small lesions or burns in a specific place. Doctors will use tools, such as fluoroscopy (x-rays) and injections to locate the specific nerves that are transmitting pain and then use the electrical current to destroy those nerves. Equipment used include generator, built in nerve stimulator, different needles and probes and water cooling system in case of the cooled RFA. There are several types of probes or needles that are used to transmit energy and create lesions. This study is going to compare 2 types - standard radiofrequency and 'cooled' radiofrequency. The only difference is that the 'cooled' radiofrequency probes have water running through the probe tip, which keeps the tip cool and allows a larger lesion to be made. Since the doctor can't actually see the nerve he is trying to target, the larger lesion should theoretically improve his chances of hitting it. The 'cooling' of the water also allows the temperatures to be lower than what is needed for standard RF. In this study, the investigators would like to compare the differences between standard RFA (90°C) and "cooled" RFA (60°C) ablation techniques and determine if one is better for pain relief. All of the probes that are used to perform radiofrequency ablation are FDA approved and are commonly used to treat patients with chronic back pain. Participating in the study involves being randomly assigned to received either standard or cooled RFA. The procedure for both standard and cooled RFA is basically the same. The only difference is with standard RFA, the doctor may perform up to 2 lesions, instead of 1 if they are using cooled RFA. Both study groups will receive local anesthetic prior to procedure. The treating doctor will use a machine called a C-Arm to take x-rays. These x-rays will guide the doctor to be sure the probes are in the right place. Once the probe placement is confirmed, the doctor will turn on the generator and create the lesion. This process will be repeated depending on how many lesions need to be created. After the procedure there will be follow up visits at 1, 3 and 6 months. Level of pain, health and recovery information will be collected.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Thoracic Back Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
c-RFA
Arm Type
Experimental
Arm Description
cooled radiofrequency ablation
Arm Title
t-RFA
Arm Type
Active Comparator
Arm Description
thermal radiofrequency ablation
Intervention Type
Procedure
Intervention Name(s)
c-RFA
Intervention Type
Procedure
Intervention Name(s)
tRFA
Primary Outcome Measure Information:
Title
Pain Score on the visual analogue scale
Time Frame
Change from baseline in pain at 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older Chronic thoracic spine mediated back pain of 3 months duration or longer Absence of focal neurologic signs or symptoms related to thoracic radiculopathy Failure to respond to conservative measures in the form of oral medication and physical therapy More than 50% reduction in their pain less than 2 months duration following a series of 2 diagnostic thoracic medial branch blocks of the affected joints using 1 ml of 1% lidocaine in the first procedure and bupivacaine 0.5 % in the second time Exclusion Criteria: Untreated coagulopathy Concomitant medical (e.g. uncontrolled cardiac condition) or psychiatric illness (e.g., untreated depression) likely to endanger the patient or compromise treatment outcomes Pregnancy Malignancy Systemic or local infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nagy Mekhail
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

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Cooled Radiofrequency Ablation vs. Thermal Radiofrequency Ablation

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