Urinary Exosomal Biomarkers of Thyroglobulin and Galectin-3 for Prognosis and Follow-up in Patients of Thyroid Cancer
1 other identifier
observational
103
1 country
1
Brief Summary
Now, the investigators carried out a prospective study enrolling patients with thyroid cancer, who had received ablative thyroidectomy and /or radioactive iodine therapy for two more years. The investigators' study already enrolled seventy-three patients with thyroid cancer, and the investigators plan to enroll 30 new patients in this consecutive research study. All patients received total thyroidectomy under clinically surgical judgement in initial therapeutic option. The investigators also further found some difference between papillary thyroid cancer and follicular thyroid cancer, and the investigators will continue annually to closely monitor the change of U-Ex Tg and urinary exosomal galectin-3 between differently cellular types of thyroid cancers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 24, 2021
CompletedFirst Posted
Study publicly available on registry
July 2, 2021
CompletedStudy Start
First participant enrolled
August 19, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 8, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2026
ExpectedApril 13, 2026
April 1, 2026
4.6 years
June 24, 2021
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (15)
Change of serum thyroglobulin level
Thyroid function test
Within 36 months
Change of serum free T4 level
Thyroid function test
Within 36 months
Change of serum TSH level
Thyroid function test
Within 36 months
Change of anti-thyroglobulin level
Thyroid function test
Within 36 months
Urinary exosomal thyroglobulin detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal galectin-3 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal calprotectin A9 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal transketolase detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal keratin 19 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal angiopoietin-1 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal tissue inhibitor of metalloproteinase detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal keratin 8 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal calprotectin A8 detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal annexin II detection
Urinary exosomal biomarker
Within 36 months
Urinary exosomal afamin detection
Urinary exosomal biomarker
Within 36 months
Eligibility Criteria
The investigators carried out a prospective study enrolling patients with thyroid cancer, who had received ablative thyroidectomy and /or radioactive iodine therapy for two more years. The study already enrolled seventy-three patients with thyroid cancer, and the investigators plan to enroll 30 new patients in this consecutive research study. All patients received total thyroidectomy under clinically surgical judgement in initial therapeutic option. The investigators also further found some difference between papillary thyroid cancer and follicular thyroid cancer, and we will continue annually to closely monitor the change of U-Ex Tg and urinary exosomal galectin-3 between differently cellular types of thyroid cancers.
You may qualify if:
- diagnosed patients with thyroid papillary, follicular and anaplastic thyroid cancer, post-operation follow up
You may not qualify if:
- unclearly diagnosed patients with thyroid papillary, follicular and anaplastic thyroid cancer
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chih-Yuan Wang, M.D
Taipei, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
CHIH-YUAN WANG, Doctor
Department of Internal Medicine, National Taiwan University Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 24, 2021
First Posted
July 2, 2021
Study Start
August 19, 2021
Primary Completion
April 8, 2026
Study Completion (Estimated)
October 31, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share