CLINICAL_TRIALS ClinicalTrials.gov record update

Investigator-Initiated Feasibility Study of a Novel Endoscopic Ultrasound Guided Microwave Ablation Device in Patients With Locally Advanced, Unresectable, or Metastatic Cancer

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT07817147
Title field or adapter rule: {'original_value': 'Investigator-Initiated Feasibility Study of a Novel Endoscopic Ultrasound Guided Microwave Ablation Device in Patients With Locally Advanced, Unresectable, or Metastatic Cancer', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At: 2026-10-31T23:27:25.855619+00:00
Published At: 2026-09-14T00:00:00+00:00
Record Updated At: 2026-09-14
Source Retrieved At: 2026-10-31T22:17:56.788771+00:00
Timestamp Basis: ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation: ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

protocolSection.conditionsModule.conditions: ["Pancreatic Cancer", "Liver Cancer (Locally Advanced or Metastatic)", "Pancreatic Cancer Non-resectable", "Pancreatic Cancer Stage III", "Pancreatic Cancer Stage IV", "Liver Cancer Stage IV", "Liver Cancer Stage IIIa", "Liver Cancer Stage IIIb", "Liver Cancer Stage IIIc"]
protocolSection.statusModule.lastUpdatePostDateStruct: {"date": "2026-09-14", "type": "ACTUAL"}
protocolSection.identificationModule.nctId: "NCT07817147"
protocolSection.identificationModule.officialTitle: "Investigator-Initiated Feasibility Study of a Novel Endoscopic Ultrasound Guided Microwave Ablation Device in Patients With Locally Advanced, Unresectable, or Metastatic Cancer"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: ["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct: null

{'armGroupLabels': ['Endoscopic Ultrasound (EUS) - Guided Microwave Ablation (MWA) Device Group'], 'description': "The rationale of this study is to generate preliminary data on the functionality and safety of Creo's MicroBlate™ Fine device when used under EUS guidance. The results generated from this study will inform any decisions regarding subsequent pivotal trials and may support the integration of this approach into clinical practice for anatomically challenging tumors.", 'name': 'EUS-Guided MWA Device', 'type': 'DEVICE'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

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