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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04623801
Other study ID # 19-438
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date October 19, 2020
Est. completion date October 2025

Study information

Verified date July 2023
Source Memorial Sloan Kettering Cancer Center
Contact R. Michael Tuttle, MD
Phone 646-608-3910
Email tuttler@mskcc.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to explore whether percutaneous laser ablation (PLA) is a safe and effective alternative to removing papillary thyroid microcarcinoma (PTMC) with surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date October 2025
Est. primary completion date October 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age = 18 years - Papillary thyroid cancer documented by - (a) Bethesda VI cytology, - (b) Bethesda III, IV, V, or VI cytology AND BRAF V600E mutation, or - (c) Bethesda V cytology AND high risk ultrasonographic features documented by either the ATA high suspicion or TIRADS 5 nodule characteristics To ensure the majority of cases will be eligible based on criteria (a) or (b), we will enroll = 2 patients based on criteria (c). - Maximum diameter = 13 mm - Declined active surveillance - The thyroid lesion must be primarily solid with = 25% cystic compent - No US evidence of extrathyroidal extension through the thyroid capsule - No imaging evidence of lymph node metastasis - Preserved contralateral vocal cord function prior to PLA Exclusion Criteria: - Thyroid cancer that is non papillary thyroid cancer (PTC) - Thyroid lesion with > 25% cystic component - Lesion with US evidence of extrathyroidal extension through the thyroid capsule - Clinical or ultrasonographic evidence of lymph node metastasis - Pregnancy

Study Design


Intervention

Procedure:
Percutaneous Laser Ablation (PLA)
Percutaneous Laser Ablation / PLA will be carried out in a single session by advancing one 21-gauge spinal needle into the target lesions under real time US guidance.

Locations

Country Name City State
United States Memorial Sloan Kettering Cancer Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with complete thermal ablation Complete thermal ablation of the targeted PTMC (T1aN0M0) as determined by histological examination of thyroid tissue obtained by either thyroid lobectomy or total thyroidectomy 6 months after PLA. 6 months
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