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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06371703
Other study ID # PETCT_INTEGO
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 2024
Est. completion date October 2024

Study information

Verified date April 2024
Source IRCCS San Raffaele
Contact Giuseppe Bonfitto
Phone 02-26438384
Email bonfitto.giuseppe@hsr.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This project aims to evaluate the impact of the introduction of an automated system for radiopharmaceutical preparation and administration on the radiation safety of the radiographers working in nuclear medicine. This study will help to fill the existing gap in the scientific literature and provide useful guidance for the selection of the safest and most effective automated infusion system.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date October 2024
Est. primary completion date October 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - 1)Nuclear medicine radiographers with experience in manual prepa-ration of radiopharmaceuticals. 2) Nuclear medicine healthcare professionals with experience in radiopharmaceutical administration. 3) Ability to provide written informed consent. Exclusion Criteria: - 1) Nuclear medicine radiographers without experience in manual preparation of radiopharmaceuticals. 2) Nuclear medicine healthcare professionals without experience in radiopharmaceutical administration. 3) Inability to provide written informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
automated system in reducing radiation exposure
evaluate the effectiveness of the automated system in reducing radiation exposure for radiographers involved in PET/CT procedures.

Locations

Country Name City State
Italy Irccs San Raffaele Milano

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in absorbed dose by radiographers during PET/CT procedures, measured in millisieverts (mSv). 3 months
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