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PKP Assisted With MR Technology in OVCF With IVC

Percutaneous Kyphoplasty Assisted With/Without Mixed Reality Technology in Treatment of OVCF With IVC: a Prospective Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03959059
Enrollment
40
Registered
2019-05-22
Start date
2017-06-15
Completion date
2018-03-20
Last updated
2019-05-22

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

Conditions

Orthopedic Disorder of Spine

Brief summary

To prospectively assess the outcome of PKP assisted with and without MR technology in treatment of OVCF with IVC.

Detailed description

The study is to prospectively assess the outcome of PKP assisted with and without MR technology in treatment of OVCF with IVC. Forty cases of OVCF with IVC undergoing PKP were randomized into a MR technology assisted group (group A) and a traditional C-arm fluoroscopy group (group B). Both groups were performed PKP and evaluated by VAS scores, ODI scores, radiological evidence of vertebral body height and kyphotic angle(KA) at pre-operation and post-operation. The volume of injected cement and Operation time was recorded. And whether cement touching both endplates or not(non-PMMA-endplates-contact, NPEC) in radiological evidence were also recorded postoperatively. The clinical outcomes and complications were evaluated afterwards. All patients received 10 to 14 months' follow-up, with an average of 12 months.

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
50 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Single level OVCF in the thoracic and lumbar levels (T10-L4), suffering with severe back pain.; * OVCF without damaged vertebral posterior wall and nerve lesion; * The patient was over 50 years old and , the diagnosis of osteopenia or osteoporosis was confirmed by bone densitometry ; * All patients underwent(received) plain radiography, computed tomography (CT) and MRI before surgery, and with IVC presented in MRI.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Kyphotic angle1 yearkyphotic angle in X-ray is also for recontruction of the vertebra.
visual analog scale1 yearvisual analog scale(0-10 scores) is for pain, 0 represent no pain, 10 score represent the severe pain.
Oswestry Disability Index1 yearOswestry Disability Index is for movement function, Questionnaire examines perceived level of disability in everyday activities of daily living. The ODI score (index) is calculated as: For example: If all 10 sections are completed, the score is calculated as follows: if 16 (total scored) out of 50 (total possible score) x 100 = 32%; If one section is missed (or not applicable), the score is calculated: If 16 (total scored) / 45 (total possible score) x 100 = 35.5%.
Vertebral height1 yearVertebral height in X-ray is for recontruction of the vertebra.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026