Your session is about to expire
← Back to Search
Procedure
RFA for Thyroid Cancer
N/A
Waitlist Available
Led By Marius Stan, MD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Radiology evaluation deems the lesion amenable to RFA therapy with minimal risk of complication
Be older than 18 years old
Must not have
Vocal cord paralysis on contralateral side
Clinical evidence for local or distant metastatic disease
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to test the effectiveness of using heat from radio waves to treat small thyroid cancers. It will focus on patients with small papillary thyroid carcinoma and will monitor changes in tumor size and other health indicators after treatment. Radiofrequency ablation (RFA) has been studied as a treatment for small papillary thyroid microcarcinomas, particularly in patients who are ineligible for surgery.
Who is the study for?
This trial is for adults with a small papillary thyroid carcinoma (less than 1.5 cm) that can be treated without surgery, as decided by their doctor and radiologist. It's not for those with widespread cancer, pregnant women, individuals who have difficult neck anatomy for RFA access, high anesthesia risk due to other illnesses, recent investigational drug use, substance abuse issues, blood clotting disorders or prior neck treatments.
What is being tested?
The study is testing Radiofrequency Ablation (RFA), which uses heat to destroy cancer cells in treating papillary thyroid carcinoma. The goal is to see how effective RFA is at eliminating the tumor while minimizing risks.
What are the potential side effects?
While the description doesn't specify side effects of RFA directly, common ones may include pain at the treatment site, swelling or bruising around the neck area where the procedure was done and potential damage to nearby structures in rare cases.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My scans show I can have RFA therapy with low risk.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My opposite side vocal cord is paralyzed.
Select...
My cancer has spread to other parts of my body.
Select...
I have been diagnosed with a type of thyroid cancer that has multiple growths.
Select...
I have had surgery or radiation treatment on my neck before.
Select...
My neck shape makes it hard for doctors to perform RFA.
Select...
I have a blood clotting disorder or am on blood thinners.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 18 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Changes in thyroid nodule size (overall volume measured in percentage)
Secondary study objectives
Development of distant metastasis
Development of lymph node involvement
Pain related to RFA procedure
+1 moreSide effects data
From 2017 Phase 1 & 2 trial • 61 Patients • NCT01853618100%
Anemia
100%
Aspartate aminotransferase increased
100%
Hyponatremia
88%
Alanine aminotransferase increased
88%
Hypoalbuminemia
88%
Alkaline phosphatase increased
88%
Lymphocyte count decreased
75%
Blood bilirubin increased
63%
Pain
63%
Platelet count decreased
63%
Rash maculo-papular
63%
Hypercalcemia
50%
Activated partial thromboplastin time prolonged
50%
White blood cell decreased
50%
Pruritus
38%
Back pain
38%
Nausea
38%
Constipation
38%
Creatinine increased
38%
Fatigue
38%
Hypophosphatemia
38%
Fever
38%
Vomiting
25%
Headache
25%
Skin hyperpigmentation
25%
Anorexia
25%
Dyspnea
25%
Generalized muscle weakness
25%
Insomnia
25%
Hyperglycemia
25%
Hypermagnesemia
25%
Hypokalemia
25%
Hyperuricemia
25%
Pleural effusion
25%
Cough
25%
Hypomagnesemia
13%
Peripheral sensory neuropathy
13%
Urinary tract infection
13%
Hyperkalemia
13%
Hypertension
13%
Neoplasms benign, malignant and unspecified (incl cysts and polyps) - Other, HCC
13%
Non-cardiac chest pain
13%
Muscle weakness left-sided
13%
Bile duct stenosis
13%
Bloating
13%
Dizziness
13%
Dysphagia
13%
Hearing impaired
13%
Hematuria
13%
Hyperhidrosis
13%
Muscle weakness upper limb
13%
Rash acneiform
13%
Sinus tachycardia
13%
Lymphocyte count increased
13%
Neutrophil count decreased
13%
Diarrhea
13%
CPK increased
13%
Gastrointestinal disorders - Other, Gastroenteritis
13%
Lung infection
13%
Dyspepsia
13%
Ascites
13%
Skin and subcutaneous tissue disorders - Other, mouth ulcers
13%
Edema limbs
13%
Seizure
13%
Eyelid function disorder
13%
Pain in extremity
13%
Productive cough
13%
Weight loss
13%
Neuralgia
13%
Urinary frequency
13%
Bone pain
13%
Paresthesia
13%
Renal and urinary disorders - Other, Dysuria
13%
Serum amylase increased
13%
Pneumothorax
13%
Abdominal distension
13%
Abdominal pain
100%
80%
60%
40%
20%
0%
Study treatment Arm
Pilot 1/Arm A1-Tremelimumab + RFA or TACE
2/Arm A2 -Tremelimumab + RFA or TACE
3/Arm B - Tremelimumab + TACE
5/Arm D - Tremelimumab + Cryoablation
6/Arm E - Tremelimumab + RFA
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: RFA GroupExperimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
RFA
2014
Completed Phase 2
~1650
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Thyroid cancer treatments primarily aim to remove or destroy cancerous cells. Surgery, such as thyroidectomy, physically removes the tumor and affected thyroid tissue.
Radioactive iodine therapy targets thyroid cells with radioactive iodine, which is absorbed by thyroid tissue and destroys cancer cells from within. External beam radiotherapy (EBRT) uses high-energy radiation to kill cancer cells and shrink tumors.
Radiofrequency ablation (RFA) involves inserting a needle into the tumor and using high-frequency electrical currents to generate heat, which destroys cancer cells. These treatments are crucial for thyroid cancer patients as they offer different approaches to effectively manage and potentially cure the disease, depending on the cancer's type, stage, and location.
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,324 Previous Clinical Trials
3,059,400 Total Patients Enrolled
Marius Stan, MDPrincipal Investigator - Mayo Clinic
Mayo Clinic Hospital-Rochester Saint Marys Campus, Mayo Clinic Rochester
University De Medical Si Farm Iuliu Hatieganu (Medical School)
Mayo Grad School Med/Mayo Fndn (Residency)
2 Previous Clinical Trials
66 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 years old or older.My opposite side vocal cord is paralyzed.Diagnosed using fine needle aspiration (FNA) testing.My cancer has spread to other parts of my body.I have been diagnosed with a type of thyroid cancer that has multiple growths.My scans show I can have RFA therapy with low risk.I have had surgery or radiation treatment on my neck before.My doctor agrees non-surgical treatment is right for me.My neck shape makes it hard for doctors to perform RFA.I have a blood clotting disorder or am on blood thinners.My thyroid nodule is identified as papillary carcinoma.I have health conditions that make general anesthesia too risky for me.The size of the condition being studied is less than 1.5 centimeters.
Research Study Groups:
This trial has the following groups:- Group 1: RFA Group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger