Actively Recruiting
Comparison of Record in VERITON Camera to the Anger Camera Procedure in Patients Treated by 131-iodine
Led by Central Hospital, Nancy, France · Updated on 2024-06-20
77
Participants Needed
1
Research Sites
121 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to show that the SPECT/CT whole body recording procedure lasting less than or equal to 30 minutes in a VERITON-CT™ camera, can be substituted for the classic procedure, giving at least equivalent information in searches for primary or metastatic neoplastic lesions.
CONDITIONS
Official Title
Comparison of Record in VERITON Camera to the Anger Camera Procedure in Patients Treated by 131-iodine
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over the age of 18 who have understood and signed the informed consent form
- Diagnosis of thyroid cancer with planned treatment by iodine 131 at 1100 MBq or 3700 MBq as approved by a multidisciplinary team
- No contraindications to undergoing the imaging examination
- Affiliation to a social security scheme
You will not qualify if you...
- Known allergy to any component of the iodine 131 capsule
- Pregnancy, breastfeeding, or women of childbearing age without suitable contraception
- Medical instability or inability to remain still in the supine position during imaging
- Legal restrictions including deprivation of liberty by judicial or administrative decision
- Adults under legal protection measures such as guardianship or curatorship
- Adults unable to provide informed consent and not under legal protection
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Chru Nancy Brabois
Vandœuvre-lès-Nancy, France, 54511
Actively Recruiting
Research Team
V
Véronique ROCH, MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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