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EUS-RFA for Pancreatic Cystic Neoplasms and Pancreatic Neuroendocrine Tumors

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Summary

NIH ClinicalTrials.gov has registered a clinical trial (NCT07536087) evaluating endoscopic ultrasound-guided radiofrequency ablation (EUS-RFA) as a treatment for pancreatic cystic neoplasms and pancreatic neuroendocrine tumors in patients ineligible for or refusing surgery. The primary endpoints assess technical feasibility and effectiveness, while secondary objectives evaluate safety and long-term efficacy including adverse events and disease progression over one year of follow-up.

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What changed

NIH ClinicalTrials.gov registered a new clinical trial (NCT07536087) titled 'Endoscopic Ultrasound-Guided Radiofrequency Ablation for Pancreatic Cystic Neoplasms and Pancreatic Neuroendocrine Tumors.' The trial will evaluate EUS-RFA as a minimally invasive therapeutic option for patients who are not suitable candidates for surgery or who decline surgical intervention.

This registry entry provides informational notice about an upcoming research study and does not create compliance obligations for healthcare providers, patients, or manufacturers. Clinical investigators conducting similar research or manufacturers of radiofrequency ablation equipment may find this trial relevant to ongoing work in this therapeutic area. The trial's outcomes may inform future treatment protocols and healthcare cost considerations for pancreatic lesion management.

Archived snapshot

Apr 17, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Endoscopic Ultrasound-Guided Radiofrequency Ablation for Pancreatic Cystic Neoplasms and Pancreatic Neuroendocrine Tumors

N/A NCT07536087 Kind: NA Apr 17, 2026

Abstract

The primary aim of this study is to evaluate the technical feasibility and effectiveness of endoscopic ultrasound-guided radiofrequency ablation (EUS-RFA) in the treatment of pancreatic cystic neoplasms (PCNs) and pancreatic neuroendocrine tumors (pNETs) in patients who are not suitable candidates for surgical treatment or who refuse surgery.

EUS-RFA, as a minimally invasive therapeutic option, may potentially reduce the need for intensive imaging surveillance, prevent further progression of these lesions, and serve as a bridging therapy in selected patients for whom surgical intervention may be considered in the future. At the same time, EUS-RFA could contribute to reducing overtreatment, thereby lowering the risk of complications associated with surgical procedures and leading to an overall reduction in healthcare costs.

The secondary objectives of the study are to evaluate the safety profile of EUS-RFA, including the incidence and severity of adverse events both in the early postoperative period and during the first year of follow-up, as well as to assess the long-term efficacy of EUS-RFA, including disease progression.

Conditions: Endoscopic Ultrasound-Guided Radiofrequency Ablation, Pancreatic Neuroendocrine Tumors (pNET), Pancreatic Cystic Neoplasms

Interventions: Endoscopic ultrasound-guided radiofrequency ablation for pancreatic cystic lesions, Endoscopic ultrasound-guided radiofrequency ablation of pancreatic solid lesions

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Last updated

Classification

Agency
NIH
Published
April 17th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07536087

Who this affects

Applies to
Clinical investigators Healthcare providers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Clinical trial registration Medical device research
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Medical Devices Public Health

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