Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:36 PM
Ignite Modification Date:
2025-12-24 @ 7:36 PM
NCT ID:
NCT06980103
Eligibility Criteria:
Inclusion Criteria:
* Patients aged 18 and older
* Patients diagnosed with intermediate risk DTC \< 6 months ago and who are making a decision about RAI treatment
* Ability to understand the information conveyed in the informed consent form, pose questions and process answers (e.g., no cognitive impairment per direct consultation with the patient's physician), and, finally, provided informed consent to participate.
* Participants willingness to be contacted and remain available to complete study activities throughout the duration of the study.
Exclusion Criteria:
* Diagnosis of low risk or high risk DTC
* Prior history of RAI
* Clinical contraindications that prevent consideration of RAI (e.g., pregnancy, lactation, neutropenia if considering high dose of RAI)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06980103
Study Brief:
Protocol Section:
NCT06980103