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Clinical Trials/NCT01269359
NCT01269359
Unknown
Not Applicable

Robotic Assisted Vertebral Body Augmentation - a Radiation Reduction Tool

Hadassah Medical Organization1 site in 1 country100 target enrollmentJanuary 4, 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Vertebral Body Augmentation
Sponsor
Hadassah Medical Organization
Enrollment
100
Locations
1
Primary Endpoint
amount of radiation
Last Updated
13 years ago

Overview

Brief Summary

Modern orthopedic and spine surgeons strive towards minimizing surgical exposure and towards increased precision in the placement of implants. This trend requires an increased use of fluoroscopic guidance, which leads to increased exposure of the patient, surgeon and the operating room staff to radiation.

Robotic assisted spine surgery is routinely performed in the authors' institution for a variety of indications such as degenerative conditions, trauma, tumors , infections and deformity correction11. The objective of this study is to compare the radiation exposure time during robotic guided vertebral body augmentation to the published results for similar surgeries.

Registry
clinicaltrials.gov
Start Date
January 4, 2011
End Date
TBD
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Men and Women
  • Ages 18-85

Exclusion Criteria

  • Unwillingness to participate the study

Outcomes

Primary Outcomes

amount of radiation

amount of radiation is calculated from the DLP (Dose Length Product)

Study Sites (1)

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