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:
2025-12-25 @ 1:06 AM
Ignite Modification Date:
2025-12-25 @ 1:06 AM
NCT ID:
NCT00085293
Eligibility Criteria:
Inclusion Criteria:
* Histologically confirmed papillary thyroid or follicular thyroid carcinoma:
* Differentiated disease;
* Metastatic disease documented by ultrasound, computed tomography (CT) scan (without iodinated contrast), or MRI - All metastatic disease foci =\< 10 mm in all dimensions
* Must have been treated with total or near-total thyroidectomy AND at least 1 course of iodine I 131 (131I)(\>=29.9 mCi) OR demonstrated negative uptake on a postoperative low-dose131I scan
* Must have undergone whole body 131I scan 1-3 days after administration of =\< 5.5 mCi of 131I demonstrating no visible iodine uptake within the lesions unless demonstrated negative uptake on a postoperative low-dose131I scan within the past 12 weeks:
* Must have 24-hour urine iodine excretion =\< 500 mcg within 1 week of 131I scan
* Must be receiving thyroid hormone therapy AND have thyroid-stimulating hormone level =\< 0.5 mU/L
* No known brain metastases
* Performance status:
* Eastern Cooperative Oncology Group (ECOG) 0-2 OR Karnofsky 60-100%
* Hematopoietic:
* Absolute neutrophil count \>= 1,500/mm3;
* Platelet count \>= 100,000/mm3;
* White Blood Count (WBC) \>= 3,000/mm3
* Hepatic:
* aspartate aminotransferase-alanine aminotransferase (AST and ALT) =\< 2.5 times upper limit of normal;
* Bilirubin normal
* Renal:
* Creatinine not elevated OR
* Creatinine clearance \>= 60 mL/min
* Cardiovascular:
* No symptomatic congestive heart failure;
* No unstable angina pectoris;
* No cardiac arrhythmia
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective contraception
* No prior allergic reaction attributed to compounds of similar chemical or biological composition to decitabine
* No concurrent uncontrolled illness
* No active or ongoing infection
* No psychiatric illness or social situation that would preclude study compliance
* No prior cytotoxic chemotherapy for thyroid cancer
* At least 6 months since prior external beam radiotherapy administered for locoregional disease in the thyroid bed or to the cervical or upper mediastinal lymph node regions (no more than 6,000 cGy)
* More than 6 months since other prior radiotherapy and recovered
* More than 6 months since prior therapeutic 131I \> 10 mCi
* More than 18 months since prior cumulative 131I activity of at least 500 mCi
* More than 12 months since prior amiodarone (Unless 24-hour urinary iodine excretion is =\< 500 mcg)
* No concurrent combination antiretroviral therapy for HIV-positive patients
* No other concurrent anticancer therapy
* No other concurrent investigational agents
* More than 6 months since prior intrathecal iodinated contrast (Unless 24-hour urinary iodine excretion is =\< 500 mcg)
* More than 3 months since prior IV or oral iodinated contrast for radiographic studies (Unless 24-hour urinary iodine excretion is =\< 500 mcg)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00085293
Study Brief:
Protocol Section:
NCT00085293