Pancreatic Insulinoma Clinical Trial
— ERASIN-RCTOfficial title:
Endoscopic Ultrasound-guided RAdiofrequency Ablation Versus Surgical Resection for the Treatment of Pancreatic INsulinoma: a Multicenter Randomized Controlled Trial
The goal of this muticentre randomized controlled trial is to compare endoscopic ultrasound-guided radiofrequency ablation (EUS-RFA) with surgery for treatment of pancreatic insulinoma. The main questions it aims to answer are: 1) What is the safest treatment? 2) Is efficacy comparable? Patients will be randomized to undergo EUS-RFA or surgical resection. Researchers will compare the rate of adverse events and the clinical efficacy after the two treatments to see if EUS-RFA result safer and effective compare with surgery.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | February 28, 2029 |
Est. primary completion date | February 28, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age =18 years - Diagnosis of pancreatic insulinoma (38) (e.g., fasting test, insulin blood levels, C-peptide blood levels) - Presence of a visible single pancreatic nodule on imaging (computed tomography, and/or magnetic resonance imaging, and/or endoscopic ultrasound). - No evidence of distant localizations visualized at computed tomography, and/or magnetic resonance imaging, and/or endoscopic ultrasound - Tumor = 2cm - Informed consent provided by the patient or closest relative. Exclusion Criteria: - G2 with Ki-67 >5% on histological examination at EUS-guided biopsy samples (if performed) - Distance between lesion and main pancreatic duct = 1mm or upstream dilation of the main pancreatic duct - Metastatic tumor at the time of diagnosis - Multiple pancreatic nodules - Diagnosis of multiple endocrine neoplasia type 1 according to guidelines - Unfit for surgery or high-risk surgical patients - Endoscopic ultrasound not feasible for surgical altered anatomy - Known bleeding disorder that cannot be sufficiently corrected with co-fact or fresh frozen plasma - Use of anticoagulants that cannot be discontinued - International normalized ratio >1.5 or platelet count <50.000 - Pregnancy or breast feeding - Failure to sign the patient's or closest relative's informed consent |
Country | Name | City | State |
---|---|---|---|
Italy | University Hospital of Verona | Verona |
Lead Sponsor | Collaborator |
---|---|
Azienda Ospedaliera Universitaria Integrata Verona |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of adverse events | Rate of overall and severe adverse events will be recorded | Up to 72 months | |
Secondary | Clinical effectiveness | Rate of patients experiencing symptoms disappearance | Up to 72 months | |
Secondary | Evaluation of quality of life by questionnaire | Assessment of quality of life using a questionnaire | Up to 72 months | |
Secondary | Length of hospital stay | Days of hospitalization | Up to 72 months | |
Secondary | Recurrence | Rate of local or distant recurrence | Up to 72 months | |
Secondary | Reintervention | Rate of reintervention | Up to 72 months | |
Secondary | Pancreatic insufficiency | Rate of endocrine or exocrine pancreatic insufficiency | Up to 72 months |
Status | Clinical Trial | Phase | |
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