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NCT04623801Active, not recruitingPhase 2

Laser Ablation of Papillary Thyroid Microcarcinoma

Pilot Study to Evaluate the Safety and Efficacy of Percutaneous Laser Ablation of Thyroid Papillary Microcarcinoma

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
10 (estimated)
First submitted
6 Nov 2020
Start date
19 Oct 2020
Primary completion date
Oct 2026
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT04623801

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 10
  • From 19 Oct 2020 to the primary completion date, Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Thyroid cancer that is non papillary thyroid cancer (PTC)

Other

  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.