Recruiting

Observational Study

Sponsor:

OAD Orthopaedics

Code:

NCT01721889

Conditions

Lumbar Degenerative Disc Disease

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Radiostereometric Analysis

Study Details

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.

Conditions

Lumbar Degenerative Disc Disease

Study ID

NCT01721889

Start date

Nov, 2012

Status verified date

Jun, 2013

Completion date

Jan, 2016

Anticipated

Primary completion date

Jan, 2015

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

30 participants

Anticipated

Interventions and Outcome Measures

Arms

Radiostereometric analysis - Intact fusion

Clinically fused per classical radiographic assessment (≤ 2 degrees angular motion and evidence of bone bridging)

Radiostereometric analysis - Symptomatic pseudoarthrosis

Definitive clinical evidence of pseudarthrosis (not fused, ˃ 2 degrees angular motion or absence of bone bridge) and scheduled for surgical exploration

Radiostereometric analysis - Asymptomatic pseudoarthrosis

Definitive clinical evidence of pseudarthrosis without scheduled surgical exploration.

Interventions

Radiostereometric Analysis

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).

Primary outcome measure

  • Intervertebral motion post-op lumbar fusion [ Time Frame: 2 years ]

Central Contacts and Locations

Central contacts

Locations

OAD Orthopaedics

Recruiting

Warrenville, Illinois, United States, 60555

Contacts

Principal Investigator:

John Andreshak, MD

More Information

Sponsor

OAD Orthopaedics

Last update posted

Jun 11, 2013

Last verified

Jun, 2013

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by OAD Orthopaedics on 2013-06-11.