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Method for bAdge-dosi Monitoring of X-ray Exposure Values in Operating Theatre Surgery
Led by University Hospital, Tours · Updated on 2025-05-29
240
Participants Needed
3
Research Sites
39 weeks
Total Duration
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AI-Summary
What this Trial Is About
Surgical procedures involving X-rays in the operating room have increased in recent years, thereby increasing the exposure of operating room staff to ionizing radiation. An individual dosimeter makes it possible to record the radiation exposure to which these personnel are exposed. However, it has been noticed that these dosimeters are not thoroughly worn, consequently the radiation doses recorded are not reliable. In order to increase the proportion of dosimeters systematically worn in the operating room, we study the impact of the association of the passive dosimeter with the hospital access badge (forming the Badge-Dosi). A first pilot study was carried out at Tours University Hospital showing the effectiveness of this concept. With the present study, we carry out a multicenter study. Our hypothesis is that the Badge-Dosi allows a significant increase of dosimeter use in the operating room, which improves the reliability of the monitoring of personnel.
CONDITIONS
Official Title
Method for bAdge-dosi Monitoring of X-ray Exposure Values in Operating Theatre Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Work in the operating room at least 80% of the time (for TEST group)
- Have been monitored by a delayed-reading dosimeter for at least 1 year (for TEST group)
- Carry a hospital access card (for TEST and LIFE groups)
- Work in the same center as the TEST group (for LIFE and HOME groups)
- Not exposed to radiation at their workstation (for LIFE group)
- Live near the center (for HOME group)
You will not qualify if you...
- Object to data processing
- Are interns, externs, or non-permanent staff likely to change jobs during the study
- Had a nuclear medicine examination within 15 days before study start
- Had internal vectorised therapy with iodine-131 or Lu-177 within 30 days before study start
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
University hospital
Orléans, France, 45000
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2
University hospital
Toulouse, France, 31000
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3
University hospital
Tours, France, 37044
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Research Team
S
Serge MAIA, Dr
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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