Comparison Between Surgical and Conservative Treatment for Lumbar Stenosis

Sponsor
Istituto Ortopedico Rizzoli (Other)
Overall Status
Completed
CT.gov ID
NCT05315466
Collaborator
(none)
30
1
2
58.3
0.5

Study Details

Study Description

Brief Summary

This study aims to compare the outcomes of surgical treatment and conservative treatment at medium- and long-term period (minimum 2 years) in patients with lumbar stenosis who come to the observation of the PI's Team at the Rizzoli Orthopaedic Institute, through a series exhaustive questionnaires to self-administer to patients in order to define a path of "decision-making" as effective as possible for the patient and the doctor.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Non-surgical treatment
  • Procedure: Surgical treatment for spinal stenosis
N/A

Detailed Description

Non-surgical treatment:

Conservative treatment may include different approaches, such as analgesics, anti-inflammatories, muscle relaxants, physical therapy, Global Postural Rehabilitation, magnetic therapy, laser therapy, TENS, massage, cognitive-behavioral therapy and all those procedures that can bring benefit in back and legs pain.

Surgical treatment:

Surgical treatment of lumbar stenosis is the decompression surgery which relieves the nerve structures to prevent permanent neurological damage. Decompression can be made on one or more segments of the spine and can be done with laminectomy, hemilaminectomy, laminotomy.

During a laminotomy part of the vertebral lamina is removed above and below the compressed nerve. The opening created is sometimes enough to relieve the compression on the nerve. In most cases, also the disc material and bone spur that compress the nerve are removed.

During a laminectomy the vertebral lamina is completely removed, along with the disc and the bone material that compress the nerves. The opening produced by the removal of the lamina is protected by back muscles and ligaments.

If the damage has occurred at several levels and bone of the vertebral support structures must be removed to achieve decompression, it can be performed a stabilization surgery with vertebral bone fusion (arthrodesis) in order to avoid instability of the column. Fusion is carried out to eliminate the mobility between different vertebrae and it is achieved using bone derived from the patient's iliac crest or from a donor. The bone gradually grows and melts with the same vertebrae. This limits the movements that may have been one of the causes of back pain. It takes about six months for it to achieve a solid bony spinal fusion.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Patients affected by lumbar spinal stenosis who are designated to surgical or conservative treatmentPatients affected by lumbar spinal stenosis who are designated to surgical or conservative treatment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison Between Surgical and Conservative Treatment for Lumbar Stenosis
Actual Study Start Date :
Aug 8, 2012
Actual Primary Completion Date :
Jun 16, 2017
Actual Study Completion Date :
Jun 16, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Non-surgical treatment

Different types of non-surgical treatments

Procedure: Non-surgical treatment
Analgesics, anti-inflammatories, muscle relaxants, physical therapy, Global Postural Rehabilitation, magnetic therapy, laser therapy, transcutaneous electrical nervous stimulation (TENS), massage, cognitive-behavioral therapy and all those procedures that can bring benefit to back and leg pain.

Experimental: Surgical treatment

Surgical treatment for spinal stenosis

Procedure: Surgical treatment for spinal stenosis
Decompression of nerve structures by laminotomy or laminectomy and posterior lumbar fusion if stabilization of the column is required.

Outcome Measures

Primary Outcome Measures

  1. Back and leg pain assessed by VAS [Change from baseline VAS at 3, 6, 12, 24 months]

    Self-administered questionnaires for patients to evaluate back and leg pain (VAS score)

  2. Functional activity assessed by ODI [Change from baseline ODI at 3, 6, 12, 24 months]

    Self-administered questionnaires for patients to evaluate a disability index (ODI)

  3. Quality of life assessed by EQ-5D [Change from baseline EQ-5D at 3, 6, 12, 24 months]

    Self-administered questionnaires for patients to evaluate the quality of life (EQ-5D)

Secondary Outcome Measures

  1. Complications [6, 12, 24 months]

    Evaluation of complications associated to the surgical treatment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Confirmatory imaging study (MRI or CT) showing lumbar spinal stenosis at one or more levels (L2 to sacrum) defined as narrowing of the central spinal canal, lateral recesses, or neural foramens due to encroachment on the neural structures by the surrounding bone and soft tissue.
Exclusion Criteria:
  • Patients are not eligible if they have evidence of instability on lateral flexion- extension radiographs, defined as a change of #10° of angulation of adjacent segments by Cobb measurement or a change of more than 4 mm of anteroposterior or posteroanterior translation.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituto Ortopedico Rizzoli Bologna Italy 40136

Sponsors and Collaborators

  • Istituto Ortopedico Rizzoli

Investigators

  • Principal Investigator: Alessandro Gasbarrini, MD, Istituto Ortopedico Rizzoli

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Istituto Ortopedico Rizzoli
ClinicalTrials.gov Identifier:
NCT05315466
Other Study ID Numbers:
  • RF MINSAL2009.STENOSI
First Posted:
Apr 7, 2022
Last Update Posted:
Apr 7, 2022
Last Verified:
Mar 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 7, 2022