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NCT Number: NCT06507085

Dosimetric Reference Levels for Radioguided Interventional Procedures in Rhythmology.

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

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:

  • Insertion of a single-chamber pacemaker with lead (DELF 007 according to the common French classification for medical acts)
  • Insertion of a dual-chamber pacemaker with lead (DELF 005 according to the common French classification for medical acts)
  • Implantation of a multi-site pacemaker (DELF 001 and/or DELF 015 according to the common French classification for medical acts)
  • Implantation of a single-chamber endovascular defibrillator (DELF 013 according to the common French classification for medical acts)
  • Implantation of a dual-chamber endovascular defibrillator (DELF 015 according to the common French classification for medical acts)
  • Placement of multi-site defibrillator (DELF 020 or DELF 014 according to the common French classification for medical acts)
  • Typical Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only (DEPF 012 according to the common French classification for medical acts)
  • Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to the common French classification for medical acts)
  • Accessory pathway ablation (DEPF 005 according to the common French classification for medical acts)
  • Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per the common French classification for medical acts)
  • Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to the common French classification for medical acts) Secondaires objectives include the evaluation of interventional practices for each procedure performed regarding the use of a fixed or mobile C-arm, the make, model and year of installation of the equipment used, deviation at last external quality control between displayed and measured dose area product and, if available, between displayed and measured Kair, the lowest/highest scan rates used during the procedure, use of graphy,lowest/highest scan rate(s) used during procedures, use of collimation during procedures, use of a 3D mapping system, the type of technique used for an ablation procedure, if used, the use of a cage-type radiation protection system during the procedure, cone beam computed tomography performed during procedure, CT scan before the procedure, duration of the procedure and the experience of the operator performing the procedure.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult male/female patient (≥ 18 years)
  • Body Mass Index (BMI) between 18 and 35 kg/m².
  • Patient to benefit from one of the following procedures:

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

  • Patient whose procedure does not require X-rays
  • Pregnant women

Treatment and study plan

Radio-guided interventions to correct heart rhythm disorders

Radiation

All patients in the cohort will be undergoing one of the following radio-guided procedures :

  • Insertion of a single-chamber pacemaker with lead
  • Insertion of a dual-chamber pacemaker with lead
  • Implantation of a multi-site pacemaker
  • Implantation of a single-chamber endovascular defibrillator
  • Implantation of a dual-chamber endovascular defibrillator
  • Placement of multi-site defibrillator
  • Typical Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only
  • Primo Ablation tachycardia by intra nodal re-entry
  • Accessory pathway ablation
  • Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined
  • Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate

Primary outcomes

  1. Radiation dose: Insertion of a single-chamber pacemaker with lead (DELF 007 according to the common French classification for medical procedures)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  2. Total Air Kerma: Insertion of a single-chamber pacemaker with lead (DELF 007 according to the common French classification for medical procedures)

    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

  3. Total scanning time: Insertion of a single-chamber pacemaker with lead (DELF 007 according to the common French classification for medical procedures)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  4. Total number of images: Insertion of a single-chamber pacemaker with lead (DELF 007 according to the common French classification for medical procedures)

    Time frame: Day 1 of the intervention

    Quantitative

  5. Radiation dose: Insertion of a dual-chamber pacemaker with lead (DELF 005 according to the common French classification for medical acts

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  6. Total Air Kerma: Insertion of a dual-chamber pacemaker with lead (DELF 005 according to the common French classification for medical acts

    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

  7. Total scanning time: Insertion of a dual-chamber pacemaker with lead (DELF 005 according to the common French classification for medical acts

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  8. Total number of images: Insertion of a dual-chamber pacemaker with lead (DELF 005 according to the common French classification for medical acts

    Time frame: Day 1 of the intervention

    Quantitative

  9. Radiation dose: Implantation of a multi-site pacemaker (DELF 001 and/or DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  10. Total Air Kerma: Implantation of a multi-site pacemaker (DELF 001 and/or DELF 015 according to the common French classification for medical acts)

    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

  11. Total scanning time: Implantation of a multi-site pacemaker (DELF 001 and/or DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  12. Total number of images: Implantation of a multi-site pacemaker (DELF 001 and/or DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  13. Radiation dose: Implantation of a single-chamber endovascular defibrillator (DELF 013 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  14. Total Air Kerma: Implantation of a single-chamber endovascular defibrillator (DELF 013 according to the common French classification for medical acts)

    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

  15. Total scanning time: Implantation of a single-chamber endovascular defibrillator (DELF 013 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  16. Total number of images: Implantation of a single-chamber endovascular defibrillator (DELF 013 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  17. Radiation dose: Implantation of a dual-chamber endovascular defibrillator (DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  18. Total Air Kerma: Implantation of a dual-chamber endovascular defibrillator (DELF 015 according to the common classification for medical acts)

    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

  19. Total scanning time: Implantation of a dual-chamber endovascular defibrillator (DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  20. Total number of images: Implantation of a dual-chamber endovascular defibrillator (DELF 015 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  21. Radiation dose: Placement of multi-site defibrillator (DELF 020 or DELF 014 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  22. Total Air Kerma : Placement of multi-site defibrillator (DELF 020 or DELF 014 according to the common French classification for medical acts)

    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

  23. Total scanning time: Placement of multi-site defibrillator (DELF 020 or DELF 014 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  24. Total number of images: Placement of multi-site defibrillator (DELF 020 or DELF 014 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  25. Radiation dose : Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only (DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 day of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  26. Total Air Kerma: Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only (DEPF 012 according to the common French classification for medical acts)

    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

  27. Total scanning time: Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only (DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  28. Total number of images: Primary Atrial Flutter Ablation: Cavotricuspid Isthmus only (DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  29. Radiation dose: Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  30. Total Air Kerma: Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to the common French classification for medical acts)

    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

  31. Total scanning time: Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  32. Total number of images: Primo Ablation tachycardia by intra nodal re-entry (DEPF 010 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  33. Radiation dose: pathway ablation (DEPF 005 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  34. Total Air Kerma: pathway ablation (DEPF 005 according to the common French classification for medical acts)

    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

  35. Total scanning time: pathway ablation (DEPF 005 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  36. Total number of images: pathway ablation (DEPF 005 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  37. Radiation dose: Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  38. Total Air Kerma: Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per the common French classification for medical acts)

    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

  39. Total scanning time: Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  40. Total number of images: Paroxysmal atrial fibrillation ablation (4 pulmonary veins only, all technologies combined; DEPF 033 as per the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

  41. Radiation dose: Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Total Dose Area Product for the procedure measured in Gy.cm2

  42. Total Air Kerma: Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to the common French classification for medical acts)

    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

  43. Total scanning time: Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    The total scanning time for the procedure will be measured in seconds

  44. Total number of images: Primo Ablation Persistent atrial fibrillation (4 pulmonary veins ± lines ± substrate; DEPF 033 ± DEPF 014 ± DENF 018 ± DEPF 012 according to the common French classification for medical acts)

    Time frame: Day 1 of the intervention

    Quantitative

Secondary outcomes

  1. Use of a fixed or mobile C-arm in each of the above 11 interventions

    Time frame: Day 1 of the intervention

    YES /NO

  2. Equipment

    Time frame: Day 1 of the intervention

    The make, model and year of commissioning the C-arm used will be recorded.

  3. Deviation between the Dose Area Product displayed and measured

    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.

  4. Deviation between the total air Kerma displayed and measured

    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.

  5. Lowest/highest fluoroscopy frame rates

    Time frame: Day 1 of the intervention

    The lowest/highest frame rates used during fluoroscopy procedures will be measured in p/s

  6. Use of fluorography

    Time frame: Day 1 of the intervention

    YES/NO

  7. Lowest /highest fluorography rates

    Time frame: Day 1 of the intervention

    The lowest/highest frame rates used during fluorography procedures will be measured in p/s

  8. Use of collimation during each of the above 11 procedures ?

    Time frame: Day 1 of the intervention

    YES/NO

  9. Use of a 3D mapping system during each of the above 11 procedures ?

    Time frame: Day 1 of the intervention

    YES/NO

  10. Technique used for ablation

    Time frame: Day 1 of the intervention

    The type of technique used for ablation procedures will be recorded

  11. Use of a collective radiation protection system during each of the above 11 procedures ?

    Time frame: Day 1 of the intervention

    YES/NO

  12. Cone Beam Computed Tomography performed during any of the procedures above ?

    Time frame: Day 1 of the intervention

    YES/NO

  13. CT scan before a paroxysmal atrial fibrillation ablation procedure ?

    Time frame: Day 1 of the intervention

    YES/NO

  14. Duration of each of the above procedures

    Time frame: Day 1 of the intervention

    The duration of each of the above procedures will be recorded in minutes

  15. Rhythmologist's experience

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Anissa MEGZARI

CONTACT

[email protected]

0466684236

Joël GREFFIER, Dr.

CONTACT

[email protected]

+334.66.68.40.68

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Nīmes

Other

Registry information

Official study title

Dosimetric Reference Levels for Radioguided Interventional Procedures in Rhythmology. The NR-Rythmo Study

Acronym: NR-Rythmo

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Jul 18, 2024
Registry last updated
Jul 18, 2024

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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