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Screws Implantation Assisted With Mixed Reality Technology

A Clinical Application Study of Mixed Reality Technology Assisted Lumbar Pedicle Screws Implantation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04062487
Enrollment
50
Registered
2019-08-20
Start date
2017-01-09
Completion date
2018-10-27
Last updated
2019-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spine Degeneration

Brief summary

Prospective comparative study of Mixed Reality Technology(MR)assisted lumbar pedicle screws placement and traditional lumbar pedicle screws placement.

Detailed description

In this study, the randomized controlled method was adopted to prospectively include the samples, and the differences in surgical procedures and efficacy were compared between the thoracolumbar pedicle screw implantation assisted by MR and the traditional thoracolumbar pedicle screw implantation, so as to provide a plan for clinicians to choose the surgical method.

Interventions

combine image with real body

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
38 Years to 53 Years
Healthy volunteers
No

Inclusion criteria

* Course of disease≥6 months, all patients with lumbago back pain, radiation pain of lower limbs, lumbar disc herniation diagnosed with or without spinal stenosis. * The course of disease≥6 months, all patients had lumbar back pain, accompanied by or without intermittent claudication, and the diagnosis of lumbar spondylolisthesis was clear, but the vertebral isthmus was not broken. * The patient's symptoms were consistent with the imaging examination results, failed to respond to conservative treatment, and met the surgical indications. * The lesion segment is no more than 3 vertebral bodies. * Preoperative improvement of X-ray, CT, MRI examination. * Patients without active bleeding and female patients is not in menstrual period.

Exclusion criteria

* Lumbar acute infection, lumbar tuberculosis, tumor and other diseases. * Patients with severe cardiopulmonary insufficiency, intolerance to surgery, diabetes and poor blood glucose control, combined with coagulation dysfunction and other contraindications. * Vertebral fracture patients. * Bone Mineral Density (BMD) examination: BMD was measured by dual-energy X- ray absorptiometry at the lumbar spine (L2 \ L4) and femoral head, and BMD and T values were observed. Abnormal bone mass were excluded according T \>- 1 SD

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale6 monthsvisual analog scale(0-10 scores) is for pain, 0 represent no pain, 10 score represent the severe pain.
Oswestry Disability Index6 monthsOswestry Disability Index is for movement function, Questionnaire examines
The Standard Of Gertzbein-Robbins1 daythe standard of Gertzbein-Robbins :Ⅰ, self-contained complete within the pedicle nail; Ⅱ, self-contained nail through 2 mm below the cortex; Ⅲ, self-contained nail through 2 mm or greater, cortex \< 4 mm; Nail through 4 mm or higher cortex; Ⅳ, self-contained, \< 6 mm; Ⅴ, self-contained nail through 6 mm or higher cortex.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026