Radiation Exposure in Spine Intervention Under Angiography

Phase 3 Study of Evaluate Radiation Exposure and Procedure Times for Continuous Fluoroscopic Monitoring During Lumbar ESI

Status

Completed

Phases

Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01751958

Enrollment

1000

Registered

2012-12-18

Start date

2011-07-31

Completion date

2012-03-31

Last updated

2012-12-18

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

Conditions

Low Back Pain

Brief summary

Evaluate radiation exposure and procedure times for continuous fluoroscopic monitoring during lumbar ESI

Detailed description

The purpose of this prospective study was to evaluate radiation exposure and procedure times for fluoroscopic monitoring during lumbar ESI with analyzing the differences among operators (experienced staff and trainee) and among different method for ESI.

Interventions

RADIATIONEpidural steroid injection

Epidural steroid injection

Study design

Allocation

NON_RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 90 Years

Healthy volunteers

Yes

Inclusion criteria

* Suspected of having radiculopathic low back pain

Exclusion criteria

* Angiography is contraindicated

Design outcomes

Primary

Measure	Time frame	Description
Radiation dose	Treatment on the day	Radiation dose of patients with spine invervention under angiography

Countries

South Korea

Outcome results

None listed

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