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Clinical Trial Summary

Scopy uses X-rays and is not without risk (deterministic and stochastic effects) for the patient and the nursing staff present in the room at the time of an endoscopic procedure requiring its use: its use must be reasoned with a benefit/risk balance in favour of carrying out the interventional procedure. In France, there is currently no multicentre study exploring the radiation doses used for each type of endoscopic procedure. Main objective: To define IRL (interventional reference levels) adapted to each type of endoscopic procedure. Secondary objective(s) : - Application of regulatory texts - Assessment of patient radiation protection - Radiation protection assessment for workers


Clinical Trial Description

Prospective data collection using an e-CRF available via Easymedstat. Data completed during the endoscopy procedure Completion of a questionnaire by the practitioner who performed the procedure afterwards, including the scopy doses used during the procedure, the type of scopy, the type of intention-to-treat ;


Study Design


NCT number NCT06363682
Study type Observational [Patient Registry]
Source Central Hospital, Nancy, France
Contact CHEVAUX Doctor CHEVAUX Jean-Baptiste, PhD
Phone +33 3 83 15 41 49
Email jb.chevaux@chru-nancy.fr
Status Not yet recruiting
Phase
Start date April 1, 2024
Completion date June 11, 2024