[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"tumor-of-pancreas\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:tumor-of-pancreas":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100537821","the-histosonics-edison-system-for-treatment-of-pancreatic-adenocarcinoma-using-histotripsy-100537821",false,"NCT06282809","The HistoSonics Edison™ System for Treatment of Pancreatic Adenocarcinoma Using Histotripsy","GANNON","Inclusion Criteria:\n\n1. Subject is ≥18 years of age.\n2. Subject has signed the Ethics Committee (EC) approved trial Informed Consent Form (ICF) prior to any trial related tests\u002Fprocedures and is willing to comply with trial procedures and required follow-up assessments.\n3. Subject is diagnosed with unresectable pancreatic adenocarcinoma (locally advanced \\[Stage 3\\] or oligometastatic disease \\[Stage 4\\]) confirmed via CT or MR imaging ≤14 days prior to the planned index procedure.\n\n   NOTE: If Stage 4 disease, there must be ≤5 metastatic tumors, the tumors must be located only in the liver and\u002For lung, and the metastatic tumors must be stable.\n4. Subject is not a surgical candidate and has received chemotherapy ≥8 weeks.\n5. Subject can tolerate general anesthesia.\n6. Subject has an Eastern Cooperative Oncology Group Performance Status (ECOG PS) grade 0-1 at baseline.\n7. Subject meets the following criteria ≤14 days prior to the planned index procedure date:\n\n   * Hemoglobin ≥ 9 g\u002FdL,\n   * Neutrophil count \\>1.0 x 10\\^9\u002FL,\n   * Platelet \\>50 x 10\\^9\u002FL,\n   * Total bilirubin ≤2.5x Institutional Upper Limit of Normal (IULN),\n   * Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤2.5x IULN,\n   * International Normalized Ratio (INR) value \\\u003C1.5,\n   * Serum creatinine \\\u003C2.0mg\u002FdL or an estimated glomerular filtration rate (eGFR) ≥45mL\u002Fmin.\n8. The targeted pancreatic tumor is ≥2 cm in longest diameter.\n9. The planned histotripsy treatment volume is ≥1.0 cm from any portion of the duodenum, small intestine, stomach, or colon as visualized on ultrasound, and CT, or MR imaging.\n10. Subject has an adequate acoustic window to visualize targeted tumor using the HistoSonics Edison System.\n11. Subject will undergo histotripsy treatment of only one (1) tumor during the index procedure, regardless of how many tumors are present in the pancreas.\n\nExclusion Criteria:\n\n1. Subject is pregnant or planning to become pregnant or nursing (lactating) during the trial period.\n2. Subject has had prior pancreatic, bilioenteric, or gastric surgery.\n3. Subject is being actively treated in another pharmaceutical or device trial that has not completed its primary endpoint prior to the index procedure or may interfere with the primary outcome measure of this trial.\n4. Subject has an uncorrectable coagulopathy.\n5. Subject has a life expectancy of less than six (6) months.\n6. Subject has a biliary or pancreatic stent and\u002For percutaneous biliary tube that encompasses the planned histotripsy treatment volume.\n7. Subject has metastases to organs other than the liver and\u002For lung (e.g., bone, brain, peritoneum).\n8. Subject has a known sensitivity to contrast media and cannot be adequately pre-medicated.\n9. Subject has an active duodenal or gastric ulcer requiring medical management.\n10. Subject is undergoing active chemotherapy for any cancer ≤7 days prior to planned index procedure date.\\*\n11. Subject is undergoing active immunotherapy or targeted therapies ≤30 days prior to planned index procedure date.\n12. Subject's targeted tumor has had prior locoregional therapy (e.g., ablation, embolization, or radiation).\n13. Subject has a planned cancer treatment (e.g., pancreatic surgery, targeted therapy, immunotherapy) exclusive of chemotherapy, ≤30 days post index procedure.\n14. Subject has planned chemotherapy ≤14 days post index procedure.\\*\n15. Subject has not recovered (CTCAE grade 2 or better) from chemotherapy or immunotherapy related toxicities (exclusive of alopecia, neuropathy, and exocrine insufficiency).\n16. In the investigator's opinion, histotripsy is not a treatment option for the subject.\n17. Subject has a concurrent condition that could jeopardize the safety of the subject or compliance with the protocol.\n18. Subject's tumor is not treatable by the System's working ranges (refer to User Guide).\n\n(\\*) Subject must not be off chemotherapy \\>21 days in total.","ALL","18 Years",{"count":19,"type":20},50,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this trial is to evaluate the safety of the HistoSonics Edison System for the destruction of pancreatic adenocarcinomas using histotripsy.",[26,27,28,29],"Pancreas Cancer","Adenocarcinoma of the Pancreas","Pancreatic Cancer","Tumor of Pancreas","RECRUITING","2026-01-14",{"date":33,"type":34},"2026-01-15","ACTUAL",{"date":36,"type":34},"2024-12-10",{"date":38,"type":20},"2027-01",{"name":40,"class":41},"HistoSonics, Inc.","INDUSTRY",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":50,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":21,"phases":54,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":42},"100528745","enucleation-of-pancreatic-tumor-by-blocking-abdominal-trunk-and-superior-mesenteric-artery-100528745","NCT06164769","Enucleation of Pancreatic Tumor by Blocking Abdominal Trunk and Superior Mesenteric Artery","A Prospective Study of Enucleation of Pancreatic Tumor by Blocking Abdominal Trunk and Superior Mesenteric Artery","Inclusion Criteria:\n\n* Benign or borderline tumors diagnosed pathologically, such as pancreatic neuroendocrine tumors, solid pseudopapillary tumors, and cystadenomas, without vascular invasion or distant metastasis\n* Tumors sited in the pancreatic head, neck, and uncinate process of pancreas\n* Blockade of both the abdominal trunk and superior mesenteric artery in the laparoscopic enucleation\n\nExclusion Criteria:\n\n* Highly malignant pancreatic tumors, or tumors with infiltration or metastasis\n* Tumors of the body and tail of the pancreas\n* Transfer to LPD or laparotomy","14 Years","70 Years",{"count":53,"type":20},30,[23],"Pancreatic enucleation could preserve more healthy pancreatic tissues and functions with a low recurrence risk. However, conventional enucleation can cause significant intraoperative bleeding, especially in which tumors in the pancreatic head, neck, and uncinate process of pancreas, as these tissues are rich in blood supply, mainly including the abdominal trunk and the superior mesenteric artery. In this study, we developed a novel method to control the pancreatic blood flow in laparoscopic enucleation--blocking the abdominal trunk and superior mesenteric artery with vascular occlusion clips in the process of resection, and evaluated its effectiveness and safety.",[29,57],"Surgical Blood Loss",[59,60,61,62,63],"Enucleation","pancreatic tumors","blood loss","the abdominal trunk","superior mesenteric artery","2025-05-27",{"date":66,"type":34},"2025-06-02",{"date":68,"type":34},"2023-03-01",{"date":70,"type":20},"2026-06-30",{"name":72,"class":73},"Zhejiang University","OTHER"]