Skip to content

Radiostereometric Analysis of Spine Arthrodesis

Radiostereometric Analysis of Spine Arthrodesis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01721889
Enrollment
30
Registered
2012-11-06
Start date
2012-11-30
Completion date
2016-01-31
Last updated
2013-06-11

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

Conditions

Lumbar Degenerative Disc Disease

Brief summary

The primary objective of this pilot study is to determine the precision of post-operative radiostereometric measurements for the assessment of lumbar spinal fusion. This study will also determine the potential for RSA as a more precise and accurate means for assessment of lumbar spinal fusion and diagnosis of pseudarthrosis.

Interventions

The radiostereometric (RSA) patient exam (flexion and extension RSA images) presents additional radiation exposure to the patient above standard of care (additional radiographs). Assuming 120kV, using three protocols (two loaded and one unloaded) per RSA exam results in a typical effective dose of approximately 2.04mSv per exam(single lumbar spine RSA at 120kV yields 0.68mSv,). HBI recommends using 140kV for lumbar spine RSA and has conducted simulations to estimate the effective dose using higher kV settings. 140kV reduces the effective dose from 0.68mSv per spine RSA to 0.2mSV, resulting in a total effective dose per RSA exam of 0.6mSv. In comparison, the estimated effective dose for a single standard lumbar spine x-ray is 1.2mSv. This additional radiation exposure is considered to be minimal risk in consideration of the number of planar x-rays the patient will undergo as part of standard care, as well as average background radiation received by humans per year (3.1mSv).

Sponsors

Halifax Biomedical Inc.
CollaboratorINDUSTRY
Central DuPage Hospital
CollaboratorOTHER
OAD Orthopaedics
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Symptomatic degenerative disc disease of the lumbar spine indication surgical intervention * Scheduled to undergo lumbar fusion surgery * Patients between the ages of 18 and 75 * Ability to give informed consent

Exclusion criteria

* Pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Intervertebral motion post-op lumbar fusion2 yearsThe purpose of this radiostereometric analysis (RSA) evaluation is to measure relative intervertebral motion in lumbar spinal fusions. Two RSA loading provocation protocols will be employed in this study; sitting and supine extension. Both loading protocols will be compard to a standard supine position which is used as an unloaded baseline protocol. Induced intervetebral motion sets will be calculated between the two loaded states, sitting and supine extension, and the unloaded state. The RSA micromotion results will be calculated and reported as translations and rotations about the three anatomic axes, maximum total point motion (MTPM) will be calculated as well.

Countries

United States

Contacts

Primary ContactMarjorie Delaney, APN
marjorie.delaney@oadortho.com630-225-2554
Backup ContactJohn Andreshak, MD
john.andreshak@oadortho.com630-225-2663

Outcome results

None listed

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