- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02638077
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
Conditions
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):
- Proportion of patients who underwent total/near-total thyroidectomy
- Proportion of patients who were treated by 131I after undergoing total/near-total thyroidectomy
- Proportion of patients who achieved serum TSH target value
- Proportion of patients who did not achieve serum TSH target value although they were treated by TSH suppression therapy
Secondary endpoint(s):
- Time to achieve serum TSH target value
- Dosage of L-T4 for patients who achieved and did not achieve serum TSH target value
- Dosage of L-T4 per kilogram of body weight for patients who achieved and did not achieve serum TSH target value
- 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
- Recurrence rate after one year follow-up
- 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
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Wuhan, Hubei, China, 430022
- Recruiting
- Wuhan Union Hospital, Tongji Medical college, Huazhong University of Science and Technology
-
Contact:
- Jie Ming
- Phone Number: 8610 027 85351622
- Email: mingjiewh@126.com
-
-
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:
- Patients who are diagnosed as DTC (the diagnosis should base on pre-operative examinations and post-operative pathology report)
- Patients who undergo the first-time thyroidectomy
- 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)
- Patients who have Chinese nationality
- Patients who have signed an informed consent form
Exclusion Criteria:
- History of thyroid surgery
- Other malignant tumors
- Severe organ damage such as heart failure of New York Heart Association classes III-IV, liverfailure, respiratory failure, renal failure, etc.
- Medical or psychological condition that would not permit the patient to complete the study or sign the informed consent
- Legal incapacity or limited legal capacity
- 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
Additional Relevant MeSH Terms
Other Study ID Numbers
- EMR200125_621
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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-
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-
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-
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-
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-
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-
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