search
Back to results

EuroPainClinicsStudy XIr-Zj (EPCS XIr-Zj)

Primary Purpose

Back Pain

Status
Active
Phase
Not Applicable
Locations
Slovakia
Study Type
Interventional
Intervention
Lumbar medial branch cryo ablation neurotomy
Lumbar medial branch radiofrequency ablation neurotomy
Endoscopic denervation of fazet joint
Sponsored by
Europainclinics z.ú.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Back Pain

Eligibility Criteria

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

Inclusion Criteria: patients aged between 20 and 80 positive two medial branch nerve blocks with pain relief over 80% during the first 12 hours after nerve block application positive patient history of facet joint pain patients with chronic low back pain for at least 6 months with back pain and leg pain (VAS >=5) those who (only if a signature was obtainable), or whose legal guardian, fully understood the clinical trial details and signed the informed consent form Exclusion Criteria: patients with a history of other spinal diseases (compression fracture, spondylitis, tumor) women with positive a pregnancy tests before the trial or who planned to become pregnant within the following 3 years other patients viewed as inappropriate by the staff disagreement with participation in the study

Sites / Locations

  • MD, PhD, FIPP Rapcan

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Lumbar medial branch cryoablation

Lumbar medial branch RF neurotomy

Lumbar fazet joint decapsulation

Arm Description

Lumbar medial branch cryoablation Procedure lumbar medial branch cryoablation Decreasing the electrode temperature to - 85 C for 120 seconds in two cycles. Follow-up: before the procedure, 3 months, 6 months, 12 months, and 24 months after the procedure Repeated cryoablation ablation procedures are allowed (when VAS will be =/> 4 ) Procedure/Surgery: Lumbar medial branch cryo ablation neurotomy A procedure based on positive lumbar Z- joint testing followed by medial branch neurotomy

Lumbar medial branch RF neurotomy Procedure lumbar medial branch RF neurotomy: Raising the temperature of the tip of the electrode to 85 C for 120 seconds. RF generator. Follow-up: before the procedure, 3 months, 6 months, 12 months, and 24 months after the procedure. Repeated cryoablation ablation procedures are allowed (when VAS will be > 4 )

Lumbar facet joint decapsulation through an endoscopic approach

Outcomes

Primary Outcome Measures

Change From Baseline EuroQoL-5 Dimension (EQ-5D) Value 6m
EQ-5D-5L self-care, usual activities, pain/discomfort and anxiety/depression
Change From Baseline EuroQoL-5 Dimension (EQ-5D) Value 12m
EQ-5D-5L self-care, usual activities, pain/discomfort and anxiety/depression
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m measured by VAS 10 point measurement
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m measured by VAS 10 point measurement
Oswestry Disability Index (ODI) 12m
The ODI self-administered questionnaire measuring 0-100 scale
Oswestry Disability Index (ODI) 6m
The ODI self-administered questionnaire measuring 0-100 scale

Secondary Outcome Measures

Full Information

First Posted
April 2, 2023
Last Updated
April 2, 2023
Sponsor
Europainclinics z.ú.
Collaborators
Slovak Academy of Sciences
search

1. Study Identification

Unique Protocol Identification Number
NCT05813639
Brief Title
EuroPainClinicsStudy XIr-Zj
Acronym
EPCS XIr-Zj
Official Title
EuroPainClinicsStudy XIr-Zj (Cryoablation vs Radiofrequency Ablation of Medial Nerve Branches of Dorsal Roots Crossing Z Joints)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 2, 2023 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
July 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Europainclinics z.ú.
Collaborators
Slovak Academy of Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Determine the efficacy of lumbar medial branch neurotomy by radiofrequency and cryoablation in patients with chronic low back pain
Detailed Description
Facet joint pain encompasses a significant portion of the possible sources of pain in patients with vertebrogenic algic syndrome.A typical symptom caused by facet joint irritation of the medial branch nerve is a back pain with intermittent irregular patchy pain spreading to the legs. The cause of this pain is irritation of the medial branch of the dorsal nerve root which innervates a facet joint. Confirmation of the source of the pain involves local anaesthetic blocks of the medial nerve branches in several adjoining vertebral areas. If this test is positive, then the patient's condition is indicated for radiofrequency ablation or cryoablation of the nerve branches. Description of interventional procedures: Patients with chronic low back pain with confirmed zygapophysial joint pain after previous two medial branch nerve blocks with positive results are indicated for radiofrequency medial neurotomy or alternative cryoablation neurotomy. Navigation with probes in both cases is arranged and directed according to fluoroscopic imaging.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospectively randomized patients with positive facet joint syndrome
Masking
Care Provider
Masking Description
sealed envelope, random software
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Lumbar medial branch cryoablation
Arm Type
Experimental
Arm Description
Lumbar medial branch cryoablation Procedure lumbar medial branch cryoablation Decreasing the electrode temperature to - 85 C for 120 seconds in two cycles. Follow-up: before the procedure, 3 months, 6 months, 12 months, and 24 months after the procedure Repeated cryoablation ablation procedures are allowed (when VAS will be =/> 4 ) Procedure/Surgery: Lumbar medial branch cryo ablation neurotomy A procedure based on positive lumbar Z- joint testing followed by medial branch neurotomy
Arm Title
Lumbar medial branch RF neurotomy
Arm Type
Experimental
Arm Description
Lumbar medial branch RF neurotomy Procedure lumbar medial branch RF neurotomy: Raising the temperature of the tip of the electrode to 85 C for 120 seconds. RF generator. Follow-up: before the procedure, 3 months, 6 months, 12 months, and 24 months after the procedure. Repeated cryoablation ablation procedures are allowed (when VAS will be > 4 )
Arm Title
Lumbar fazet joint decapsulation
Arm Type
Experimental
Arm Description
Lumbar facet joint decapsulation through an endoscopic approach
Intervention Type
Procedure
Intervention Name(s)
Lumbar medial branch cryo ablation neurotomy
Intervention Description
The procedure is based on positive lumbar Z- joint testing followed by medial branch neurotomy
Intervention Type
Procedure
Intervention Name(s)
Lumbar medial branch radiofrequency ablation neurotomy
Intervention Description
The procedure is based on positive lumbar Z- joint testing followed by medial branch neurotomy
Intervention Type
Procedure
Intervention Name(s)
Endoscopic denervation of fazet joint
Intervention Description
The procedure is based on positive lumbar Z- joint testing followed by decapsulation of the facet joint through an endoscopic approach
Primary Outcome Measure Information:
Title
Change From Baseline EuroQoL-5 Dimension (EQ-5D) Value 6m
Description
EQ-5D-5L self-care, usual activities, pain/discomfort and anxiety/depression
Time Frame
6 months follow-up
Title
Change From Baseline EuroQoL-5 Dimension (EQ-5D) Value 12m
Description
EQ-5D-5L self-care, usual activities, pain/discomfort and anxiety/depression
Time Frame
12 months follow-up
Title
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m
Description
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m measured by VAS 10 point measurement
Time Frame
6 months follow-up
Title
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m
Description
Change From Baseline Visual Analog Pain Scale (VAS) of Back Pain 6m measured by VAS 10 point measurement
Time Frame
12 months follow-up
Title
Oswestry Disability Index (ODI) 12m
Description
The ODI self-administered questionnaire measuring 0-100 scale
Time Frame
12 months follow-up
Title
Oswestry Disability Index (ODI) 6m
Description
The ODI self-administered questionnaire measuring 0-100 scale
Time Frame
6 months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients aged between 20 and 80 positive two medial branch nerve blocks with pain relief over 80% during the first 12 hours after nerve block application positive patient history of facet joint pain patients with chronic low back pain for at least 6 months with back pain and leg pain (VAS >=5) those who (only if a signature was obtainable), or whose legal guardian, fully understood the clinical trial details and signed the informed consent form Exclusion Criteria: patients with a history of other spinal diseases (compression fracture, spondylitis, tumor) women with positive a pregnancy tests before the trial or who planned to become pregnant within the following 3 years other patients viewed as inappropriate by the staff disagreement with participation in the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MD, PhD, FIPP Rapcan, MD, FIPP
Organizational Affiliation
R-Clinic Bardejov, Slovakia, 085 01
Official's Role
Study Chair
Facility Information:
Facility Name
MD, PhD, FIPP Rapcan
City
Bardejov
ZIP/Postal Code
08501
Country
Slovakia

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
publishing results

Learn more about this trial

EuroPainClinicsStudy XIr-Zj

We'll reach out to this number within 24 hrs