NCT05752604

Brief Summary

DTC has a generally favorable prognosis. The possibility to discriminate between patients with aggressive tumors and those with a more indolent behavior may reduce the need for unnecessary treatments. Aim of this observational study is to evaluate how anamnestic, clinical, and histopathological variables may influence the outcome of the enrolled patients, both regarding morbidity and mortality and in terms of therapeutic choices. The study aims to evaluate the prognostic impact of the therapeutic interventions in terms of efficacy and regarding the appearance of adverse events.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
3,000

participants targeted

Target at P75+ for all trials

Timeline
192mo left

Started Jul 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress19%
Jul 2022Mar 2042

Study Start

First participant enrolled

July 12, 2022

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

February 17, 2023

Completed
13 days until next milestone

First Posted

Study publicly available on registry

March 2, 2023

Completed
9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 8, 2032

Expected
10 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 8, 2042

Last Updated

August 3, 2025

Status Verified

August 1, 2025

Enrollment Period

9.7 years

First QC Date

February 17, 2023

Last Update Submit

August 1, 2025

Conditions

Outcome Measures

Primary Outcomes (9)

  • Dynamic risk stratification

    impact of the different variables on the DRS

    one year from the primary treatment

  • Dynamic risk stratification

    impact of the different variables on the DRS

    five years from the primary treatment

  • Dynamic risk stratification

    impact of the different variables on the DRS

    ten years from the primary treatment

  • Progression-free survival

    impact of the different variables on the PFS in patients treated with TKI for advanced thyroid cancer

    one year from the primary treatment

  • Progression-free survival

    impact of the different variables on the PFS in patients treated with TKI for advanced thyroid cancer

    five years from the primary treatment

  • Progression-free survival

    impact of the different variables on the PFS in patients treated with TKI for advanced thyroid cancer

    ten years from the primary treatment

  • Overall survival

    impact of the different variables on the OS in patients treated with TKI for advanced thyroid cancer

    one year from the primary treatment

  • Overall survival

    impact of the different variables on the OS in patients treated with TKI for advanced thyroid cancer

    five years from the primary treatment

  • Overall survival

    impact of the different variables on the OS in patients treated with TKI for advanced thyroid cancer

    ten years from the primary treatment

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all consecutive patients referred to our tertiary clinical center for thyroid cancer

You may qualify if:

  • \- thyroid cancer diagnosis

You may not qualify if:

  • patients unable to sign informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Istituto Auxologico Italiano, IRCCS

Milan, 20149, Italy

RECRUITING

MeSH Terms

Conditions

Thyroid Neoplasms

Condition Hierarchy (Ancestors)

Endocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsHead and Neck NeoplasmsEndocrine System DiseasesThyroid Diseases

Central Study Contacts

Laura Fugazzola, MD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 17, 2023

First Posted

March 2, 2023

Study Start

July 12, 2022

Primary Completion (Estimated)

March 8, 2032

Study Completion (Estimated)

March 8, 2042

Last Updated

August 3, 2025

Record last verified: 2025-08

Locations