Initial Management in Patients With Differentiated Thyroid Cancer in the Real World in China (DTCC)

December 18, 2015 updated by: Tao Huang, Huazhong University of Science and Technology

A Multi-center, Prospective Study to Observe the Initial Management of Patients With Differentiated Thyroid Cancer in the Real World in China (DTCC Study)

  • To find out the gap between real-world clinical practice and guideline recommendations in initial management of DTC patients
  • To observe the characteristics of patients who achieved and did not achieve TSH target value after one year follow-up
  • To assess response to initial therapy in patients who undergo total or near-total thyroidectomy and RAI remnant ablation after one year follow-up (according to an modified dynamic risk stratification system)
  • To observe the recurrence status after one year follow-up

Study Overview

Status

Unknown

Detailed Description

Multi-center, prospective, registry study

2000 DTC patients undergo the first-time thyroidectomy and identified as intermediate or high risk of recurrence will be recruited. Doctors can treat the patients based on disease conditions. Investigators will record data which are related to study endpoints.

Primary endpoint(s):

  1. Proportion of patients who underwent total/near-total thyroidectomy
  2. Proportion of patients who were treated by 131I after undergoing total/near-total thyroidectomy
  3. Proportion of patients who achieved serum TSH target value
  4. Proportion of patients who did not achieve serum TSH target value although they were treated by TSH suppression therapy

Secondary endpoint(s):

  1. Time to achieve serum TSH target value
  2. Dosage of L-T4 for patients who achieved and did not achieve serum TSH target value
  3. Dosage of L-T4 per kilogram of body weight for patients who achieved and did not achieve serum TSH target value
  4. Proportion of excellent response/Acceptable response/Biochemical incomplete response/Structural incomplete response to initial management in patients who undergo total or near-total thyroidectomy and RAI remnant ablation after one year follow-up
  5. Recurrence rate after one year follow-up
  6. AEs related to L-T4 (or thyroid tablet)treatment

Study Type

Observational

Enrollment (Anticipated)

2000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Hubei
      • Wuhan, Hubei, China, 430022
        • Recruiting
        • Wuhan Union Hospital, Tongji Medical college, Huazhong University of Science and Technology
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Differentiated Thyroid Cancer patients undergo the first-time thyroidectomy and identified as intermediate or high risk of recurrence will be recruited.

Description

Inclusion Criteria:

  1. Patients who are diagnosed as DTC (the diagnosis should base on pre-operative examinations and post-operative pathology report)
  2. Patients who undergo the first-time thyroidectomy
  3. Patients who are identified as intermediate-risk or high-risk of recurrence after thyroidectomy (according to the recurrence risk stratification of Chinese management guideline for patients with thyroid nodules and differentiated thyroid cancer published in 2012)
  4. Patients who have Chinese nationality
  5. Patients who have signed an informed consent form

Exclusion Criteria:

  1. History of thyroid surgery
  2. Other malignant tumors
  3. Severe organ damage such as heart failure of New York Heart Association classes III-IV, liverfailure, respiratory failure, renal failure, etc.
  4. Medical or psychological condition that would not permit the patient to complete the study or sign the informed consent
  5. Legal incapacity or limited legal capacity
  6. Unwilling to be followed up

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Group 1
2000 DTC patients undergo the first-time thyroidectomy and identified as intermediate or high risk of recurrence will be recruited. Doctors can treat the patients based on disease conditions. Investigators will record data which are related to study endpoints.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Proportion of patients who underwent total/near-total thyroidectomy
Time Frame: one year
one year
2. Proportion of patients who were treated by 131I after undergoing total/near-total thyroidectomy
Time Frame: one year
one year
Proportion of patients who achieved serum TSH target value
Time Frame: one year
one year
4. Proportion of patients who did not achieve serum TSH target value although they were treated by TSH suppression therapy
Time Frame: one year
one year

Secondary Outcome Measures

Outcome Measure
Time Frame
Time to achieve serum TSH target value
Time Frame: one year
one year
Dosage of L-T4 for patients who achieved and did not achieve serum TSH target value
Time Frame: one year
one year
3. Dosage of L-T4 per kilogram of body weight for patients who achieved and did not achieve serum TSH target value
Time Frame: one year
one year
4. Proportion of excellent response/Acceptable response/Biochemical incomplete response/Structural incomplete response to initial management in patients who undergo total or near-total thyroidectomy and RAI remnant ablation after one year follow-up
Time Frame: one year
one year
Recurrence rate after one year follow-up
Time Frame: one year
one year
AEs related to L-T4 (or thyroid tablet)treatment
Time Frame: one year
one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2015

Primary Completion (Anticipated)

April 1, 2017

Study Completion (Anticipated)

April 1, 2017

Study Registration Dates

First Submitted

December 18, 2015

First Submitted That Met QC Criteria

December 18, 2015

First Posted (Estimate)

December 22, 2015

Study Record Updates

Last Update Posted (Estimate)

December 22, 2015

Last Update Submitted That Met QC Criteria

December 18, 2015

Last Verified

December 1, 2015

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Not yet

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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