Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03974256
Other study ID # PHRIP2018/AUTOTEC-GRIGNON-AS
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date July 1, 2024

Study information

Verified date August 2021
Source Central Hospital, Nancy, France
Contact Rachel GRIGNON, Technologist
Phone +33 383155423
Email r.grignon@chru-nancy.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The radiopharmaceuticals manipulation used in nuclear medicine department is a significant source of radiation for operators. According to Article R. 4451-13 of the Labor Code, the exposure limit for hands and skin (average dose over a surface of 1 cm²) received during twelve consecutive months can't exceed the annual dose limit 500 millisieverts (mSv). The radiopharmaceuticals manipulation exposes operators to the risk of exceeding this limit, as has been shown in a European study. At present, there are automatons on the market but only for radiopharmaceutical fluorodeoxyglucose (FDG). One of the advantages of such an automaton is to reduce irradiation of operators' hands during the radiopharmaceuticals preparation. This reduction can reach 95% according to certain authors and the type of automaton. This study therefore proposes to evaluate the effect of an original, newly designed automaton on operators' dosimetry and the labelled radiopharmaceuticals' quality. The hypothesis emitted in this study is that the use of this automaton would allow to reduce drastically operators' hands exposure and probably also to improve the precision of the prepared syringes. This study will be done in a paired way, require a randomization in cross-over and each of the subjects included will be its own witness.


Description:

Currently, radiopharmaceuticals for diagnostic purposes are prepared by operators, Technologist in Medical Electro-Radiology or/and Pharmacy Technicians, manually for radiopharmaceuticals labelled with Technetium-99m (99mTc), or using an automaton for radiopharmaceuticals FDG. At present, there are automatons on the market but only for radiopharmaceuticals FDG. However, these automatons are currently only used to split into individual doses radiopharmaceuticals FDG, the labelling radiopharmaceuticals being carried out before delivery in nuclear medicine departments. The Sysark SAS's company has created and patented, with the collaboration of the Center of Research in Automatic Control of Nancy (CRAN, mixed unite of research 7039 common to the University of Lorraine and the CNRS) an innovative automaton for the preparation of radiopharmaceuticals labelled with 99mTc, used to perform scintigraphy examinations of nuclear medicine department.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 22
Est. completion date July 1, 2024
Est. primary completion date January 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult (age > 18 years) - Operators: Technologist in Electro-Radiology Medical / Pharmacy Technician - Operators experienced and autonomous in labelling radiopharmaceuticals with technetium-99m, at least one year - Operators having agreed to participate in the study, having received complete information on the organization of the research and having signed a free and informed consent - Operators affiliated to a social security scheme or beneficiary of such a scheme Exclusion Criteria: - A woman of childbearing age who doesn't have effective contraception - Persons referred in Articles L. 1121-5, L 1121-8 of the French Public Health Code: - Pregnant woman, parturient or mother who is breastfeeding - Chil (not emancipated) - Adult subject to a measure of legal protection (guardianship, curators, safeguard of justice) - Adult unable to express consent - Persons deprived of their liberty by a judicial or administrative decision, persons under psychiatric care pursuant to Articles L. 3212-1 and L. 3213-1

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Training in the use of the automaton
2 days training on automaton use

Locations

Country Name City State
France CHRU Nancy - Brabois Vandoeuvre-les-Nancy

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total radiopharmaceutical activity prepared in mega-becquerel (MBq) For each of the two methods of preparation Throughout 4 working days of each methods
Primary Number of days of handling For each of the two methods of preparation Throughout 4 working days of each methods
Secondary Accuracy in terms of activity (MBq) of prepared syringes, expressed as a percentage (%) of the prescribed target value, and compared between the automated device and the conventional manual method For each of the two methods of preparation Throughout 4 working days of each methods
Secondary A likert of 4 modalities will be used to evaluate the level of comfort in the automaton by operators (from "Very uncomfortable" to "Very comfortable") During the automated method of preparation After 4 working days of this method
Secondary A likert of 4 modalities will be used to evaluate the confidence level in the automaton by operators (from "Not at all confident" to "Totally confident") During the automated method of preparation After 4 working days of each methods
Secondary Level of operators' irradiation, measured by the breast dosimeter during the 4 days of preparation (in µSv) and expressed in relation to the total radiopharmaceuticals' activity prepared during the same period (in MBq) For each of the two methods of preparations Throughout 4 working days of each methods