Monitoring of Fluoroscopy Time on the Dose Delivered to the Patient During Vertebral Cementoplasty Procedures

Interest of Continuous Monitoring of the Fluoroscopy Time on the Dose Delivered to the Patient During Vertebral Cementoplasty Gestures With a Flat Panel Detector

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06174077

Acronym

CIMVER

Enrollment

Registered

2023-12-18

Start date

2020-10-06

Completion date

2023-12-31

Last updated

2023-12-18

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

Conditions

Vertebra Compression Fracture

Keywords

Vertebra Compression Fracture, Vertebral cementoplasty, Fluoroscopy time, Fluoroscopic control, Single-level vertebral cementoplasty

Brief summary

The interventional radiology department of the Strasbourg University Hospital performs approximately 1,000 vertebral cementoplasties per year. This is one of the most practiced procedures in the department and therefore exposes the professionals in the room to significant annual cumulative doses of irradiation. The objective of the study is to evaluate the interest of continuous visual monitoring of the fluoroscopy time by the operator on the dose delivered to the patient during an interventional radiology procedure performed under fluoroscopic control. The chosen reference examination is a single-level vertebral cementoplasty, a standardized examination that is frequent enough to allow easy data collection

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Adult patient (≥18 years old) * Man or woman * Patient cared for at the HUS in interventional service for the realization of a vertebral cementoplasty of a single level between 01/06/2020 and 30/09/2020 * Subject who has not expressed his opposition, after being informed, to the reuse of his data for the purposes of this research.

Exclusion criteria

* Patient who expressed their opposition to the reuse of their data for research purposes * Vertebroplasties of more than one level * History of spinal surgery or vertebroplasty near the level concerned

Design outcomes

Primary

Measure	Time frame
Assess the interest of continuous visual monitoring of the fluoroscopy time by the operator on the dose delivered to the patient during an interventional radiology procedure performed under fluoroscopic control	up to 1 month

Countries

France

Contacts

Primary ContactRoberto Luigi CAZZATO, MD

robertoluigi.cazzato@chru-strasbourg.fr33 3 69 55 16 35

Outcome results