Nîmes University Hospital
Nîmes, Gard, 30029, France
Location status: Recruiting
NCT Number: NCT06507085
Interventional radiology has become a widespread technique used in various fields of medicine to diagnose or treat numerous pathologies. However, the risk of X-rays must be taken into account. In 2019, the French Authority on Nuclear Safety published diagnostic reference levels for radio-guided interventional practices for 10 interventional radiology procedures and 2 interventional cardiology procedures, based on studies published by the French Society of Medical Physics in collaboration with the French Society of Radiology and the French Coronary Artery Disease and Interventional Cardiology Group. Reference levels for interventional procedures under CT guidance were also defined in 2020 following a national multicenter study coordinated by Nîmes University Hospital (NIMAO NRD-SI). However, no national multicentre studies have ever defined reference levels for radioguided interventional procedures in rhythmology. The aim of this study is to define standard national dosimetric levels for a number of radioguided interventional procedures in rhythmology.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Nîmes, Gard, 30029, France
Location status: Recruiting
Interventional radiology has become a widespread technique used in various fields of medicine to diagnose or treat numerous pathologies. However, the risk of X-rays must be taken into account.
To provide healthcare professionals with an optimization tool, the International Commission on Radiological Protection (ICRP) introduced the concept of diagnostic reference levels (DRLs) in 1997. For the first time, in 2019, the French Authority on Nuclear Safety published DRLs for radio-guided interventional practices for 10 interventional radiology procedures and 2 interventional cardiology procedures, based on studies published by the French Society of Medical Physics in collaboration with the French Society of Radiology and the French Coronary Artery Disease and Interventional Cardiology Group. Reference levels for interventional procedudures under CT guidance were also defined in 2020 following a national multicentre study coordinated by Nîmes University Hospital (NIMAO NRD-SI). However, no national multicentre studies have ever defined reference levels for radioguided interventional procedures in rhythmology. The aim of this study is to define standard national diagnostic reference levels for radioguided interventional procedures in rhythmology for the following acts:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Placement of single-chamber pacemaker with lead (DELF 007 according to CCAM) Dual-chamber pacemaker insertion with lead (DELF 005 according to CCAM) Multi-site pacemaker placement (DELF 001 and/or DELF 015 according to CCAM) Placement of single-chamber endovascular defibrillator (DELF 013 according to CCAM) Placement of dual-chamber endovascular defibrillator (DELF 015 according to CCAM) Placement of multi-site defibrillator (DELF 020 or DELF 014 according to CCAM) Primo Ablation Typical Atrial Flutter: Cavotricuspid Isthmus only (DEPF 012 according to CCAM) Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to CCAM) Accessory pathway ablation (DEPF 005 according to CCAM) Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per CCAM) Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to CCAM)
Exclusion criteria
All patients in the cohort will be undergoing one of the following radio-guided procedures :
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 day of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
Total Dose Area Product for the procedure measured in Gy.cm2
Time frame: Day 1 of the intervention
The total Air Kerma for the procedure will be measured at the interventional reference point (Kair) in Gy
Time frame: Day 1 of the intervention
The total scanning time for the procedure will be measured in seconds
Time frame: Day 1 of the intervention
Quantitative
Time frame: Day 1 of the intervention
YES /NO
Time frame: Day 1 of the intervention
The make, model and year of commissioning the C-arm used will be recorded.
Time frame: Day 1 of the intervention
The date of the last mandatory Quality Control and deviation between the Dose Area Product displayed and actually measured will be recorded.
Time frame: Day 1 of the intervention
The date of the last mandatory Quality Control and deviation between the total air Kerma displayed and actually measured will be recorded.
Time frame: Day 1 of the intervention
The lowest/highest frame rates used during fluoroscopy procedures will be measured in p/s
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
The lowest/highest frame rates used during fluorography procedures will be measured in p/s
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
The type of technique used for ablation procedures will be recorded
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
YES/NO
Time frame: Day 1 of the intervention
The duration of each of the above procedures will be recorded in minutes
Time frame: Day 1 of the intervention
The number of years of experience of the surgeon who performed the procedure will be recorded in years
Contact information is provided by the study sponsor or research team.
Anissa MEGZARI
CONTACT
Joël GREFFIER, Dr.
CONTACT
Centre Hospitalier Universitaire de Nīmes
Other
Dosimetric Reference Levels for Radioguided Interventional Procedures in Rhythmology. The NR-Rythmo Study
Acronym: NR-Rythmo
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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