An observational study in Thyroid Nodules and Pulsed Field Ablation, sponsored by M.D. Anderson Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-01.
Sponsored by M.D. Anderson Cancer Center · Observational
To observe the outcomes of nsPFA therapy to treat benign thyroid nodules.
Primary Objectives
Secondary Objectives
207 studies on the registry are indexed under Thyroid Nodule; 64 are open to participants now.
This study's planned enrollment of 30 is below the median of 161 across 82 observational studies indexed under Thyroid Nodule.
Browse Thyroid Nodule studies →M.D. Anderson Cancer Center is the lead sponsor of 3,047 studies on the registry; 578 are open to participants now.
Of its 612 completed or terminated interventional studies of FDA-regulated products, 409 (67%) have results posted.
Counted across the registry records on this site, refreshed daily.
MD Anderson Cancer Center
Eligibility Criteria
Presence of -confirmed benign thyroid nodule , defined as one of the following:
Exclusion Criteria
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
Biopsy and archival tissue
A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.
Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
patient-reported outcomes questionnaire
Quality-of-life Questionnaire
Time frame: Through study completion; an average of 1 year
Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.
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