Minuteman Spinal Fusion Implant Versus Surgical Decompression for Lumbar Spinal Stenosis

NCT01455805 | Completed DMC

• 1 other identifier: SS2011UK
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 4

Brief Summary

Lumbar spinal stenosis (LSS), is a common disorder of narrowing of the spinal canal in the lower part of the back. This causes discomfort in the legs when standing or walking because of pressure on the spinal nerves.There are several treatment options for LSS including physiotherapy, lumbar surgical decompression procedures such as laminectomy, Foraminotomy, Discectomy and more recently devices for interspinous distraction such as the XSTOP® and from May 2011 Minuteman™. Surgical decompression for LSS involves the removal of excess bone, ligament, and soft-tissue allowing more room for the nerves. The operation is usually preformed under general anaesthetic and with an average stay in hospital for 2-3 nights. Whereas the Minuteman™ implant is preformed as a day case under local or general anaesthetic and involves implanting the device into the space between two back bones to relieve pressure on the nerves and, therefore, pain in the legs. This is a multi centred (four sites) randomised controlled trial with a total sample of 50 participants after obtaining their informed consent. Participants will attend the pain clinic at the Hospitals for a baseline visit where they will be randomised with a ratio of 1:1 to receive either the Minuteman™ Interspinous interlaminar fusion Implant or standard surgical decompression for the treatment of lumbar spinal stenosis (LSS). Following randomisation arrangements will be made for the participant to receive the randomised treatment. If allocated to Minuteman™ Implant, the treatment will be conducted by the Pain Specialist identified at the site. If allocated to surgical decompression, the treatment will be conducted by the neuro/spinal-surgeon identified at the site. Participates will be followed up regularly for 60 months post implant to assess clinical efficacy, safety, participants function and quality of life of each treatment.

Conditions

Lumbar Spinal Stenosis; Spondylolisthesis; Degenerative Disc Disease

Outcome Measures

Primary Outcomes (1)

• Change from baseline of clinical efficacy up to 60 months post procedure

  These include: * Visual Analogue Scale (VAS) pain scores Leg Pain * Visual Analogue Scale (VAS) pain scores Back Pain * Oswestry Disability Index (ODI) * Zurich Claudication Questionnaire (ZCQ) * Assessment of Physical Function via distance walked in 5 minutes and number of repetitions of sitting to standing in 1 minute. The main outcome will be a comparison between treatment groups based on the change from baseline at each follow-up visit for each of the measures listed above.

  8 weeks and up to 60 months post procedure.

Secondary Outcomes (2)

• measures of quality of life

  8 weeks and up to 60 months post procedure.

• Adverse events related to device and procedure

  safety to be assessed at 8 weeks and up to 60 months post procedure.

Study Arms (2)

Minuteman Fusion Implant

ACTIVE COMPARATOR

Minuteman™ interspinous interlaminar fusion Implant (interspinous interlaminar fusion device) which gained CE Mark approval in May 2011

Device: Minuteman Fusion Implant

Surgical decompression

OTHER

Surgical decompression refers to the following operations Laminectomy, Foraminotomy, Discectomy or any other surgical procedure that the clinician feels is relevant for the decompression of lumbar spinal stenosis.

Procedure: surgical decompression

Interventions

Minuteman Fusion Implant DEVICE

The Minuteman™ interspinous interlaminar fusion device consists of a central threaded portion that has a two-part wing plate hinged near its proximal end, with spikes on the extended distal end of the wing plate, and a multi-spiked end cap plate that is located at the distal end of the device and is retained and tightened in place with a locking hex nut. Compression between the spiked wing plate and the spiked end cap plate serves to fix the spinous processes in place and to facilitate fusion, together with bone graft fusion material placed within the device. The threaded external body has been designed to provide ease of distraction and insertion via a minimally invasive surgical procedure.

Also known as: The Minuteman™ interspinous interlaminar fusion device

Minuteman Fusion Implant

surgical decompression PROCEDURE

Surgical decompression refers to the following operations Laminectomy, Foraminotomy, Discectomy or any other surgical procedure that the clinician feels is relevant for the decompression of lumbar spinal stenosis

Surgical decompression

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Is male or a non pregnant female aged 18years or older
• BMI ≤ 35kg/m2
• Has chronic leg pain with or without back pain of greater than 6 months duration,which is partially or completely relieved by either sitting or adopting a flexed posture and who are suitable in the clinicians opinion for posterior lumbar surgery
• Pre-operative ODI score ≥ 20%
• Pre-operative ZCQ Physical Function Domain ≥2
• Pre-operative VAS Leg pain score ≥ 4
• Has completed at least 6 months of conservative treatment without obtaining adequate symptomatic relief or has worsening neurological symptoms.
• Has degenerative changes at 1 or 2 levels confirmed by MRI or CT Myelogram within the last 12 months) with one or more of the following:
• Lumbar spinal stenosis with intermittent neurogenic claudication
• Degeneration of the disc (as evidenced by imaging on MRI)
• Annular thickening
• Degenerative Spondylolisthesis ≤ Meyerding Grade 1
• Thickening of ligamentum flavum

You may not qualify if:

• Fixed motor deficit
• Has undergone previous lumbar spinal surgery
• Is unwilling or unable to give consent or adhere to the follow up schedule
• Has active infection or metastatic disease
• Has spondylolisthesis \> grade 1
• Has neurogenic bladder or bowel disease
• Has a history of Osteopenia and or Osteoporosis. Evaluation of possible Osteopenia and or Osteoporosis will be conducted via a bone density scan prior to randomisation if ANY of the Bone Mass Evaluation criteria is met
• Patients who are not deemed fit for anaesthesia/major surgery due to underlying medical condition

Sponsors & Collaborators

• Spinal Simplicity LLC: lead
• The Leeds Teaching Hospitals NHS Trust: collaborator

Study Sites (4)

Taunton & Somerset NHS Foundation Trust of Musgrove Park Hospital

Taunton, Somerset, TA1 5DA, United Kingdom

Location

The Ipswich Hospital NHS Trust

Ipswich, Suffolk, IP4 5PD, United Kingdom

Location

Pain and Interventional Neuromodulation Research Group, Pain Management Dept, Seacroft Hospital, Leeds Teaching Hospitals NHS Trust

Leeds, West Yorkshire, LS14 6UH, United Kingdom

Location

The Dudley Group NHS Foundation Trust, Russell Hall Hospital

Birmingham, DY1 2HQ, United Kingdom

Location

MeSH Terms

Conditions

Spinal Stenosis; Spondylolisthesis; Intervertebral Disc Degeneration

Interventions

Decompression, Surgical

Condition Hierarchy (Ancestors)

Spinal Diseases; Bone Diseases; Musculoskeletal Diseases; Spondylolysis; Spondylosis

Intervention Hierarchy (Ancestors)

Surgical Procedures, Operative

Study Officials

• Ganesan Baranidharan, Dr

  Leeds Teaching Hospitals NHS Trust

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 13, 2011
• First Posted: October 20, 2011
• Study Start: June 1, 2012
• Primary Completion: March 1, 2024
• Study Completion: March 1, 2024
• Last Updated: April 11, 2024

Record last verified: 2024-04

Locations

GB (4)