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Study identifier: NCT07287176 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Prospective Evaluation of the Pulse Biosciences nPulse™ Vybrance™ Percutaneous Electrode System

Condition: Thyroid Nodule · Thyroid Goiter · Ablation  ·  Sponsor: Pulse Biosciences, Inc.

PhaseNA
Planned participants100
Who can joinAll sexes, 22 Years to 80 Years
Healthy volunteersNo

About this study

The primary objective of this study is to reproduce in a multi-center study results obtained during the feasibility First-In-Human (FIH) study with Prof. Stefano Spiezia, MD (Ospedale del Mare, Naples, Italy) and to monitor additional thyroid-related symptoms and impact of patients quality of life post-ablation using a validated QoL questionnaire.

This description comes directly from the study's public registry record.

Talk to the study team

Ioana Gruchevska  ·  (314) 484-7033  ·  ioana.gruchevska@pulsebiosciences.com

William A. Knape  ·  9197572033  ·  bknape@pulsebiosciences.com

Always discuss trial participation with your own doctor first.

Locations (3)

Sarasota Memorial HospitalSarasota, Florida, United StatesRecruiting
NYU Langone HealthNew York, New York, United StatesRecruiting
Weill Cornell MedicineNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07287176