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Radiofrequency Nucleoplasty vs Percutaneous Nucleotomy vs Decompression Catheter in Lumbar Disc Herniation

Primary Purpose

Herniated Disc

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Nucleoplasty
Percutaneous decompression
Intervertebral electrothermal disc decompression (IDET)
Conservative treatment
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Herniated Disc focused on measuring contained lumbar herniated disc, nucleoplasty, percutaneous decompression, Dekompressor, intervertebral electrothermal disc decompression, IDET

Eligibility Criteria

18 Years - 54 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: History of concordant radicular leg pain unresponsive to conservative treatment for longer than 3 months Leg pain must be greater than back pain Contained disc herniation as evidenced by MRI No evidence of psychological issues by exam or history Exclusion Criteria: A score of greater than 10 on Beck Depression Inventory (BDI) Patients with pending workers compensation claim or litigation Pregnancy Tumor Systemic infection or localized infection at the anticipated entry needle site Traumatic spinal fracture History of coagulopathy Unexplained bleeding Progressive neurological deficits History of opioid abuse or patients currently on long acting opioids Patients presenting with moderate or severe lumbar central or lateral canal stenosis, free disc fragments or degenerative disc disease as described on MRI

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    Experimental

    Arm Label

    Nucleoplasty

    Percutaneous decompression

    Electrothermal disc decompression (IDET)

    Behavioral:Conservative treatment

    Arm Description

    Procedure/Surgery: Nucleoplasty

    Procedure/Surgery: Percutaneous decompression

    Procedure/Surgery: Intervertebral electrothermal disc decompression (IDET)

    Conservative treatment with oral medications, physical therapy, epidural steroid injections

    Outcomes

    Primary Outcome Measures

    VAS pain evaluation score at baseline, 1, 3, 6, 9, 12 months

    Secondary Outcome Measures

    Oswestry results
    Disability Index
    Quality of Life SF-36
    SF-36 score at baseline 1, 3, 6, 9, 12 months
    Return to work evaluation
    Return to work evaluation
    Depression score
    Beck Depression Inventory score at pre-treatment visit
    Opioid use
    Opioid use

    Full Information

    First Posted
    March 8, 2006
    Last Updated
    May 2, 2022
    Sponsor
    The Cleveland Clinic
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00300898
    Brief Title
    Radiofrequency Nucleoplasty vs Percutaneous Nucleotomy vs Decompression Catheter in Lumbar Disc Herniation
    Official Title
    Radiofrequency Nucleoplasty vs Percutaneous Nucleotomy (Dekompressor) vs Decompression Catheter for the Treatment of Painful Contained Lumbar Disc Herniation: A Prospective Randomized Controlled Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2022
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Unable to enroll
    Study Start Date
    July 2006 (Actual)
    Primary Completion Date
    August 2007 (Actual)
    Study Completion Date
    August 2007 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The Cleveland Clinic

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to learn which of three minimally invasive procedures is the most effective for treatment of contained lumbar disc herniation.
    Detailed Description
    Contained herniation of the lumbar intervertebral disc is a frequent cause of leg and back pain. Over the last decade, there is a tendency to shift from surgical treatment of the intervertebral disc including laminectomy/discectomy to an excess of nonoperative management. Three techniques introduced recently are used as minimally invasive treatments for decompression of contained herniation of the nucleus pulposus. Nucleoplasty uses Coblation® radiofrequency vaporization of nuclear tissue to decompress the intervertebral disc. Catheter disc decompression uses heat from a resistive coil positioned in the area of disc herniation while Dekompressor® uses volume reduction to decrease an intradiscal pressure. This is a comparison study which investigates if intervertebral electrothermal disc decompression produces better pain relief measured on VAS scale, improvement in functional capacity, return to work and opioid use, than nucleoplasty or percutaneous disc decompression (Dekompressor) of the lumbar intervertebral disc in a prospective randomized controlled study. Patients will be randomized into four treatment groups in equal numbers. The first group will be treated using nucleoplasty, the second will receive Dekompressor® lumbar disc decompression, the third will receive thermal treatment using decompression catheter (Achutherm TM) and the forth will be the control group. The control group will be treated conservatively using medications including gabapentin, a breakthrough opioid (oxycodone 5 mg 1-2 tablets q 4-6 hours as needed), NSAID, epidural steroid injections and physical therapy. Patients will be followed and assessed at one, three, six, nine and twelve months following the procedure using VAS scores, Oswestry and SF-36 Short Form questionnaires, opioid use and return to work evaluation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Herniated Disc
    Keywords
    contained lumbar herniated disc, nucleoplasty, percutaneous decompression, Dekompressor, intervertebral electrothermal disc decompression, IDET

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Nucleoplasty
    Arm Type
    Active Comparator
    Arm Description
    Procedure/Surgery: Nucleoplasty
    Arm Title
    Percutaneous decompression
    Arm Type
    Active Comparator
    Arm Description
    Procedure/Surgery: Percutaneous decompression
    Arm Title
    Electrothermal disc decompression (IDET)
    Arm Type
    Active Comparator
    Arm Description
    Procedure/Surgery: Intervertebral electrothermal disc decompression (IDET)
    Arm Title
    Behavioral:Conservative treatment
    Arm Type
    Experimental
    Arm Description
    Conservative treatment with oral medications, physical therapy, epidural steroid injections
    Intervention Type
    Procedure
    Intervention Name(s)
    Nucleoplasty
    Intervention Type
    Procedure
    Intervention Name(s)
    Percutaneous decompression
    Intervention Type
    Procedure
    Intervention Name(s)
    Intervertebral electrothermal disc decompression (IDET)
    Intervention Type
    Behavioral
    Intervention Name(s)
    Conservative treatment
    Primary Outcome Measure Information:
    Title
    VAS pain evaluation score at baseline, 1, 3, 6, 9, 12 months
    Time Frame
    baseline 1, 3, 6, 9, 12 months
    Secondary Outcome Measure Information:
    Title
    Oswestry results
    Description
    Disability Index
    Time Frame
    baseline 1, 3, 6, 9, 12 months
    Title
    Quality of Life SF-36
    Description
    SF-36 score at baseline 1, 3, 6, 9, 12 months
    Time Frame
    baseline 1, 3, 6, 9, 12 months
    Title
    Return to work evaluation
    Description
    Return to work evaluation
    Time Frame
    1 month
    Title
    Depression score
    Description
    Beck Depression Inventory score at pre-treatment visit
    Time Frame
    BASELINE
    Title
    Opioid use
    Description
    Opioid use
    Time Frame
    1, 3, 6, 9, 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    54 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: History of concordant radicular leg pain unresponsive to conservative treatment for longer than 3 months Leg pain must be greater than back pain Contained disc herniation as evidenced by MRI No evidence of psychological issues by exam or history Exclusion Criteria: A score of greater than 10 on Beck Depression Inventory (BDI) Patients with pending workers compensation claim or litigation Pregnancy Tumor Systemic infection or localized infection at the anticipated entry needle site Traumatic spinal fracture History of coagulopathy Unexplained bleeding Progressive neurological deficits History of opioid abuse or patients currently on long acting opioids Patients presenting with moderate or severe lumbar central or lateral canal stenosis, free disc fragments or degenerative disc disease as described on MRI
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Leonardo Kapural, MD, OhD
    Organizational Affiliation
    Cleveland Clinic Foundation, Pain Management Department
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Radiofrequency Nucleoplasty vs Percutaneous Nucleotomy vs Decompression Catheter in Lumbar Disc Herniation

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