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Trial Title:
Cryoablation of Benign Thyroid Nodules: a Pilot Study
NCT ID:
NCT06014229
Condition:
Benign Thyroid Nodule
Conditions: Official terms:
Thyroid Nodule
Thyroid Diseases
Study type:
Interventional
Study phase:
N/A
Overall status:
Active, not recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Intervention model description:
pilot study
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Device
Intervention name:
cryoablation
Description:
Single session with an argon-based cryoablation device; an specific applicator will be
used for the treatments; gas release 100% for cryoablation; local anesthesia or moderate
sedation or general anesthesia at discretion of the anesthesiology / interventional
radiology team; benign thyroid nodules (two benign cytological examinations) measuring
between 5 and 65 mL of volume and less than 40% of cystic component;
Arm group label:
Cryoablation
Summary:
This study will evaluate the clinical response and safety of ultrasound guided
percutaneous cryoablation in the treatment of benign thyroid nodules as an alternative to
the surgery. Ablation of functioning or non-functioning benign thyroid nodules with
cryoablation will be directed to patients with symptomatic benign thyroid lesions (two
benign cytological examinations) measuring between 5 and 65 mL of volume and less than
40% of cystic component; patients must present with serum free thyroxine (T4) and thyroid
stimulating hormone (TSH) between the normal range values, with no signs of thyroiditis
by serum antibodies over 100% of the standard values; calcitonin levels in the normal
range values. Cryoablation will be directed to patients in a non-randomized fashion.
Clinical, laboratorial and imaging monitoring will be performed in 12 months, including
contrast-enhanced ultrasound when indicated, by 1, 3, 6 and 12 months.
Detailed description:
Palpable nodular thyroid disease is common in up to 6.4% of the population, and it
becomes more common when the thyroid is examined by ultrasound. The vast majority of
nodules are benign and, over time, do not change considerably in size. The main treatment
indications for a euthyroid patient with a benign thyroid nodule that is not
hyperfunctioning are compression of the trachea or esophagus, growth of the nodule, and
recurrence of a cystic nodule after aspiration. Other indications for treatment are neck
discomfort, cosmetic concern, and patient anxiety about the lump. The main therapeutic
options are surgery (unilateral lobectomy) and treatment with thyroxine. Thermal ablative
therapy has become a treatment option for solid thyroid lesions, with extensive reports
in the medical literature on safety and efficacy with laser and radiofrequency devices,
including long-term follow-up studies (10 years). There is no record in the medical
literature of the use of cryoablation devices for the ablation of benign thyroid nodules,
although they are used for the treatment of tumor lesions in different sites (hepatic,
renal, pulmonary, bone and cervical lymph nodes).The objective of this research is to
evaluate, in a pilot study, the safety and efficacy of cryoablation in the treatment of
benign thyroid nodules.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- 18 years of age or older
- Patients with solitary or dominant functioning or non-functioning thyroid nodules
with two consecutive fine needle aspiration biopsy (FNAb)-proven benign in the last
12 months
- Thyroid nodules should be solid or almost solid (less than 40% of liquid component)
with volume between 5 and 65 cc;
- Patients considered high surgical risk candidates or patients are eligible to
surgery who are informed about the ablation therapy and prefers it instead surgery;
- Calcitonin, thyroglobulin or TSH serum levels in the normal range values
Exclusion Criteria:
- Age under 18 years
- Extensive goiter
- Predominantly cystic nodule with small solid remnant (less than 10%)
- Nodule volume > 65 cc
- TSH levels above the normal range
- Uncorrectable coagulopathy / impossibility to interrupt anticoagulants;
- Malignant or suspected malignant cytologic specimens;
- Pregnancy or breast-feeding;
- Anaplastic or poor-differentiated thyroid carcinoma;
- Partial thyroidectomy
- Asymptomatic patients
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
University of Sao Paulo General Hospital
Address:
City:
São Paulo
Country:
Brazil
Start date:
August 24, 2023
Completion date:
April 30, 2025
Lead sponsor:
Agency:
University of Sao Paulo General Hospital
Agency class:
Other
Source:
University of Sao Paulo General Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06014229