Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nuclectomy 3 (LOPAIN3)

• ClinicalTrials.gov Identifier: NCT05732818
• Recruitment Status: Recruiting
• First Posted: February 17, 2023
• Last Update Posted: February 17, 2023
• Sponsor: Spinal Stabilization Technologies
• Collaborator: Raylytic GmbH
• Information provided by (Responsible Party): Spinal Stabilization Technologies

Tracking Information

• First Submitted Date: January 30, 2023
• First Posted Date: February 17, 2023
• Last Update Posted Date: February 17, 2023
• Actual Study Start Date: November 4, 2022
• Estimated Primary Completion Date: November 4, 2026 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: February 7, 2023)

Safety: Number of Patients with Serious Adverse Events related to the PerQdisc [ Time Frame: 12 months ]

Freedom from device- and procedure-related serious adverse events definitely related to the PerQdisc Device or the PerQdisc Surgical Procedure

• Original Primary Outcome Measures: Same as current
• Change History: No Changes Posted

Current Secondary Outcome Measures (submitted: February 7, 2023)

• Performance: ODI [ Time Frame: 3 months ]
  Change in Oswestry Disability Index (ODI) comparing baseline to follow up visits using a patient reported outcome tool
• Performance: ODI [ Time Frame: 6 months ]
  Change in Oswestry Disability Index (ODI) comparing baseline to follow up visits using a patient reported outcome tool
• Performance: ODI [ Time Frame: 12 months ]
  Change in Oswestry Disability Index (ODI) comparing baseline to follow up visits using a patient reported outcome tool
• Performance: ODI [ Time Frame: 24 months ]
  Change in Oswestry Disability Index (ODI) comparing baseline to follow up visits using a patient reported outcome tool
• Performance: VAS Back [ Time Frame: 3 months ]
  Change in back pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Back [ Time Frame: 6 months ]
  Change in back pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Back [ Time Frame: 12 months ]
  Change in back pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Back [ Time Frame: 24 months ]
  Change in back pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Leg [ Time Frame: 3 months ]
  Change in leg pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Leg [ Time Frame: 6 months ]
  Change in leg pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Leg [ Time Frame: 12 months ]
  Change in leg pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: VAS Leg [ Time Frame: 24 months ]
  Change in leg pain values as measured by the 100 millimeter Visual Analog Scale (VAS)
• Performance: Analgesic Score [ Time Frame: 3 months ]
  Change in level of pain medication used comparing baseline to follow up visits based on a medication scale from 0 (no meds) to 4 (high dose opioids)
• Performance: Analgesic Score [ Time Frame: 6 months ]
  Change in level of pain medication used comparing baseline to follow up visits based on a medication scale from 0 (no meds) to 4 (high dose opioids)
• Performance: Analgesic Score [ Time Frame: 12 months ]
  Change in level of pain medication used comparing baseline to follow up visits based on a medication scale from 0 (no meds) to 4 (high dose opioids)
• Performance: Analgesic Score [ Time Frame: 24 months ]
  Change in level of pain medication used comparing baseline to follow up visits based on a medication scale from 0 (no meds) to 4 (high dose opioids)
• Safety: Number of Patients with Reherniation/recurrent disc herniation [ Time Frame: 3 months ]
  Freedom from reherniation/recurrent disc herniation
• Safety: Number of Patients with Reherniation/recurrent disc herniation [ Time Frame: 6 months ]
  Freedom from reherniation/recurrent disc herniation
• Safety: Number of Patients with Reherniation/recurrent disc herniation [ Time Frame: 12 months ]
  Freedom from reherniation/recurrent disc herniation
• Safety: Number of Patients with Reherniation/recurrent disc herniation [ Time Frame: 24 months ]
  Freedom from reherniation/recurrent disc herniation
• Safety: Number of Patient that Received Supplemental fixation [ Time Frame: 3 months ]
  Freedom from supplemental fixation at the index level(s) including basivertebral nerve ablation, radiofrequency ablation or spinal cord stimulator
• Safety: Number of Patient that Received Supplemental fixation [ Time Frame: 6 months ]
  Freedom from supplemental fixation at the index level(s) including basivertebral nerve ablation, radiofrequency ablation or spinal cord stimulator
• Safety: Number of Patient that Received Supplemental fixation [ Time Frame: 12 months ]
  Freedom from supplemental fixation at the index level(s) including basivertebral nerve ablation, radiofrequency ablation or spinal cord stimulator
• Safety: Number of Patient that Received Supplemental fixation [ Time Frame: 24 months ]
  Freedom from supplemental fixation at the index level(s) including basivertebral nerve ablation, radiofrequency ablation or spinal cord stimulator

• Original Secondary Outcome Measures: Same as current

Current Other Pre-specified Outcome Measures (submitted: February 7, 2023)

• Exploratory Endpoint: Disch Height [ Time Frame: 3 months ]
  Disc height in millimeters at each clinical visit as measured on plain film X-ray
• Exploratory Endpoint: Disch Height [ Time Frame: 6 months ]
  Disc height in millimeters at each clinical visit as measured on plain film X-ray
• Exploratory Endpoint: Disch Height [ Time Frame: 12 months ]
  Disc height in millimeters at each clinical visit as measured on plain film X-ray
• Exploratory Endpoint: Disch Height [ Time Frame: 24 months ]
  Disc height in millimeters at each clinical visit as measured on plain film X-ray
• Exploratory Endpoint: RoM [ Time Frame: 3 months ]
  Preservation of range of movement (expressed in degrees) at the index and adjacent levels at baseline compared to follow-up using flexion/extension radiographs
• Exploratory Endpoint: RoM [ Time Frame: 6 months ]
  Preservation of range of movement (expressed in degrees) at the index and adjacent levels at baseline compared to follow-up using flexion/extension radiographs
• Exploratory Endpoint: RoM [ Time Frame: 12 months ]
  Preservation of range of movement (expressed in degrees) at the index and adjacent levels at baseline compared to follow-up using flexion/extension radiographs
• Exploratory Endpoint: RoM [ Time Frame: 24 months ]
  Preservation of range of movement (expressed in degrees) at the index and adjacent levels at baseline compared to follow-up using flexion/extension radiographs
• Exploratory Endpoint: Neurological Status [ Time Frame: 3 months ]
  Maintenance and/or improvement of baseline neurologic status through physical assessment evaluating nerve compression at baseline and post-surgical follow-up using pain, motor strength, and sensation feedback from the patient on a 0 (no compression) to 5 (major compression) scale
• Exploratory Endpoint: Neurological Status [ Time Frame: 6 months ]
  Maintenance and/or improvement of baseline neurologic status through physical assessment evaluating nerve compression at baseline and post-surgical follow-up using pain, motor strength, and sensation feedback from the patient on a 0 (no compression) to 5 (major compression) scale
• Exploratory Endpoint: Neurological Status [ Time Frame: 12 months ]
  Maintenance and/or improvement of baseline neurologic status through physical assessment evaluating nerve compression at baseline and post-surgical follow-up using pain, motor strength, and sensation feedback from the patient on a 0 (no compression) to 5 (major compression) scale
• Exploratory Endpoint: Neurological Status [ Time Frame: 24 months ]
  Maintenance and/or improvement of baseline neurologic status through physical assessment evaluating nerve compression at baseline and post-surgical follow-up using pain, motor strength, and sensation feedback from the patient on a 0 (no compression) to 5 (major compression) scale

• Original Other Pre-specified Outcome Measures: Same as current

Descriptive Information

• Brief Title: Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nuclectomy 3
• Official Title: Clinical Investigation Plan First in Human Trial Lumbar Operatively Inserted PerQdisc Artificial Implant Following Nuclectomy "LOPAIN3"
• Brief Summary: This study is a First in Human, prospective, multi-center clinical study intended to collect safety and performance information for the Spinal Stabilization Technologies PerQdisc® Nucleus Replacement System and procedure concurrently following a successful discectomy using a minimally invasive posterolateral (MIPL) approach. Patients that are at least 21 years or older, presenting with symptomatic radiculopathy from a focal lumbar disc herniation that requires surgical decompression will be included in this study.

Detailed Description

The PerQdisc® Nucleus Replacement System is comprised of an in situ formed silicone-based prosthesis with its delivery system, implant fill device, dispenser gun, a disc access system and two different imaging balloons. For this trial, the PerQdisc® will be implanted using minimally invasive posterolateral (MIPL) approach. The implanted device provides an effective means of replacing dysfunctional nucleus pulposus while supporting the native annulus fibrosis to bridge annular defects.

Patients that suffer clinically significant lumbar disc herniations currently undergo discectomy procedures to relieve nerve root compression. The standard discectomy procedure does not correct the annular defect associated with the herniation and is associated with a risk for re-herniation. In addition, the progressive loss of disc height and overall lack of disc turgor and weight bearing capacity is thought to be associated with downstream degenerative changes that may lead to chronic low back pain and premature spondylosis.

• Study Type: Interventional
• Study Phase: Not Applicable

Study Design

Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description:

Patients will receive one implant if they meet all inclusion/exclusion criteria after a review by the Medical Advisory Board (MAB).

Masking: None (Open Label)
Primary Purpose: Treatment

Condition

• Back Pain With Radiation
• Radiculopathy
• Back Pain
• Disc Herniation
• Herniated Nucleus Pulposus
• Herniated Disc
• Disc Injury
• Disk Herniated Lumbar

Intervention

Device: PerQdisc Nucleus Replacement System

Lumbar spine disc nucleus replacement system. All patients meeting all inclusion criteria and no exclusion criteria will be considered for nucleus replacement surgery following a review by the Medical Advisory Board.

Study Arms

Experimental: Lumbar Disc Nucleus Replacement following discectomy

All patients meeting all inclusion criteria and no exclusion criteria will be considered for nucleus replacement surgery following a review by the Medical Advisory Board.

Intervention: Device: PerQdisc Nucleus Replacement System

• Publications *: Not Provided

Recruitment Information

• Recruitment Status: Recruiting
• Estimated Enrollment (submitted: February 7, 2023): 50
• Original Estimated Enrollment: Same as current
• Estimated Study Completion Date: April 1, 2027
• Estimated Primary Completion Date: November 4, 2026 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

• Patient is skeletally mature and at least 21 years of age.
• Patient has a lumbar disc herniation, between L1-S1, with compressive radiculopathy of the traversing nerve root requiring partial discectomy or sequestrectomy. Only one lumbar disc may be treated with the PerQdisc device.
• Patient must have an overall disc herniation (extrusion or protrusion) such that half or less of the width of the dorsal annulus of the spinal canal, is affected by the herniation. The width of the canal is defined by the lateral recesses and the central canal (i.e. pedicle to pedicle).
• Patient must have a minimum of 6 mm of disc height as measured in the center of the affected disc.
• Patient is willing and able to give informed consent.
• All surgeries must be approved by at least 2 members of the Medical Advisory Board (MAB) - potential anatomical limitations of safely accessing Kambin's, extent of annular disruption, as well as overall patient criteria will be evaluated

Exclusion Criteria:

• Patient has had prior lumbar spine surgery at the index level (nucleoplasy is acceptable).
• Patient has had spinal fusion in the lumbar spine. Cervical or thoracic fusion is allowed as long as there are no neurologic deficits in the lower extremities.
• Patient has spondyloarthropathy or other spondylolisthesis greater than 4 mm or spondylolysis at the index level (on standing X-ray).
• Patient has underlying moderate or severe spinal stenosis (congenital, degenerative, or due to epidural lipomatosis) at any level. If the index level shows stenosis due to the disc herniation, it is acceptable if the index level is going to be treated concurrently with the PerQdsic procedure.
• Patient has compressive radiculopathy of the exiting nerve root at the index level.
• Patient has significant facet disease. Significant is defined as clinically confirmed by diagnostic block or radiologically grade 2 or higher (mild joint narrowing and irregularity are acceptable, but not sclerosis or osteophyte formation).
• Patient has any known active malignancy.
• Patient has previously undergone or currently on immunosuppressive therapy. Steroids used to treat inflammation are allowed.
• Patient has active local or systemic infection.
• Patient has been diagnosed with hepatitis, rheumatoid arthritis, lupus erythematosus, or other autoimmune disease including AIDS, AIDS related complex (ARC) and HIV.
• Patient has diabetes mellitus (Type 1 or 2) requiring daily insulin management.
• Patient has osteopenia of the spine (T-score of -1.0 or lower). All patients 50 years of age or older, and any post menopausal women with a history of fractures should have a dual x-ray absorptiometry (DEXA) scan to confirm exclusion.
• Patient has morbid obesity defined as a body mass index (BMI) more than 35 (>35).
• Patient has a known allergy to silicone or barium sulfate.
• Patient has a broad disc herniation that is wider than ½ of the dorsal annulus forming the wall of the spinal canal
• Patient requires decompression involving disruption of the midline bony-ligamentous elements (i.e. laminectomy).
• Patient has a significant Schmorl's node at the level to be treated, or any Schmorl's nodes affecting 3 or more lumbar levels. Significant is defined as a large, rectangular or irregular shaped node that has an associated active inflammatory process (Modic I changes).
• Patient has more than 20 degrees of mobility on flexion/extension radiographs at the index level
• Patient has more than 10 degrees of lumbar scoliosis.
• Patient belongs to a vulnerable population or has a condition such that his/her ability to provide informed consent, comply with follow-up requirements, or provide self-assessments is compromised (e.g. developmentally disabled, prisoner, chronic alcohol/ substance abuser)
• Patient is pregnant or plans to become pregnant during the course of the study. Pregnancy ruled out by serum HCG. If patient becomes pregnant during the course of the study and wishes to continue study participation, a new Pregnancy Informed Consent must be completed.

Intraoperative Exclusion:

• Poor radiological visualization of Kambin's triangle
• Patient has annular defect following surgical treatment of the disc herniation/protrusion that is greater than 6 mm
• Sustained irritation of the exiting nerve root during any aspect of the annular dilation technique (leg movement or if performing with electrical monitoring) in spite of repositioning instruments.
• Protrusion of the 50A Imaging Balloon up to or beyond the outer margin of the vertebra during the imaging steps.
• Patient has a violated endplate as determined by imaging balloons during fluoroscopy.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 21 Years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Listed Location Countries: Paraguay

Administrative Information

• NCT Number: NCT05732818
• Other Study ID Numbers: DPQ114.B: LOPAIN3
• Has Data Monitoring Committee: Yes

U.S. FDA-regulated Product

• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No

• IPD Sharing Statement: Not Provided
• Current Responsible Party: Spinal Stabilization Technologies
• Original Responsible Party: Same as current
• Current Study Sponsor: Spinal Stabilization Technologies
• Original Study Sponsor: Same as current
• Collaborators: Raylytic GmbH
• Investigators: Not Provided
• PRS Account: Spinal Stabilization Technologies
• Verification Date: February 2023