Papillary Thyroid Microcarcinoma Clinical Trial
Official title:
RFA Treatment for Papillary Thyroid Microcarcinoma Cohort
NCT number | NCT05189821 |
Other study ID # | AAAT6770 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | November 1, 2021 |
Est. completion date | November 2026 |
Thyroid surgery has always been the mainstay of treatment for thyroid cancer. Thyroid surgery carries a low risk of complications that include recurrent or superior laryngeal nerve injury leading to voice changes, hypoparathyroidism, hypothyroidism with need for thyroid hormone supplementation, and unsightly scarring. Although many patients with thyroid cancer find these risks acceptable, these risks are sometimes less acceptable to patients with benign disease. In an era when the medical field is treating thyroid diseases less aggressively, there is a pressing need to identify approaches to treat indolent malignant disease less invasively. The purpose of this observational study is to evaluate the efficacy and safety of Radiofrequency Ablation (RFA) for treatment of Papillary Thyroid Microcarcinoma (PTMC) in patients that have already agreed to RFA procedure based on treating physician recommendation. This is a data collection study in which we ask participants to give us access to information generated before and after RFA treatment of their condition. The RFA procedure uses image guidance to place an electrode through the skin into the target tumor. In RFA, high-frequency electrical currents are passed through an electrode, creating a small region of heat to treat the lesion.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | November 2026 |
Est. primary completion date | November 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Adult patients (>/= 18 years) - Biopsy proven papillary thyroid microcarcinoma (>/= 1.5cm in greatest diameter, PTMC) - Either refuse surgery or are not good surgical candidates Exclusion Criteria: - Cardiac arrhythmia - Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University |
United States,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Complete sonographic disappearance (CD) | Rate of complete sonographic disappearance of primary tumor s/p RFA | 12 months | |
Secondary | Complications | Procedural complications s/p RFA including but not limited to infection, bleeding, nerve injury, structural injury | 12 months |
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