[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Creo Medical Limited\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":64},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,44],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":26,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100569072","bronchoscopic-microwave-ablation-of-lung-tissue-in-surgical-candidates-100569072",false,"NCT06689488","Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates","Assessment of the Safety and Performance of the AB1 Electrosurgical System for Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates","AB1MALTISC","Inclusion Criteria:\n\nPatients who:\n\n1. Have signed informed consent.\n2. Subject is willing and able to comply with all aspects of the treatment and evaluation schedule.\n3. Are ≥ 18 years old.\n4. Have lung lesion(s)\u002Fnodule(s) which are histopathological-confirmed as cancer.\n5. Have soft tissue lung lesion(s):\n\n   * ≤ 30 mm in the largest dimension of the pulmonary window for Stage A.\n   * ≤ 20 mm in the largest dimension of the pulmonary window for Stage B.\n6. Are candidates for surgical resection as determined by a multi-disciplinary team (MDT) or tumour board.\n7. Greater than 10 mm of tumour-free lung parenchyma between target tumour and pleura or fissure.\n8. Subject is willing and able to comply with the study protocol requirements.\n9. Are assigned an ASA (American Society of Anaesthesiologists) score of ≤ 3 or the patient is deemed fit for general anaesthesia.\n\nExclusion Criteria:\n\nPatients who:\n\n1. Have target nodule(s) within the International Association for the Study of Lung Cancer (IASLC) \"Central Zone\" (including bronchial tree, major vessels, heart, oesophagus, spinal cord, and phrenic \\& laryngeal nerves).\n2. Are pregnant or breast feeding, as determined by standard site practices.\n3. Have participated in an investigational drug or device research study within 30 days of enrolment that would interfere with this study.\n4. Have a physical or psychological condition that would impair study participation or jeopardise the safety or welfare of the subject.\n5. Have an expected survival less than 12 months.\n6. Have bleeding diathesis, uncorrectable coagulopathy, or platelet count ≤ 100 x 10\\^9\u002FL.\n7. Have an implantable device, including pacemakers or other electronic implants.\n8. Have known pulmonary hypertension (PASP \\[pulmonary artery systolic pressure\\] \\>50mmHg).\n9. Who are currently prescribed anticoagulants, clopidogrel or other platelet aggregation inhibitors which can´t be stopped or temporarily withheld.\n10. Subject had a prior pneumonectomy.\n11. Diagnosis of Small Cell Lung Cancer.\n12. Any patient with clinically significant interstitial lung disease in the zone of planned ablation.\n13. Subject had a therapeutic intervention (e.g., SBRT) within same lobe as the target lesion.\n14. Subjects currently undergoing or underwent chemotherapy, systemic immunosuppressive treatment, or radiotherapy within 3 months of planned Study procedure.","ALL","18 Years",{"count":20,"type":21},30,"ESTIMATED","OBSERVATIONAL","The overall purpose of this study is to characterise the clinical safety and performance of the Creo Medical MicroBlate™ Flex AB1 instrument in patients with pathologically confirmed malignancy eligible for surgical resection of their nodule, receiving bronchoscopic ablation prior to surgery.",[25],"Lung Cancer",[27,28,29,30],"Bronchoscopy","Ablation","Microwave","Lung cancer","RECRUITING","2026-06-23",{"date":34,"type":35},"2026-06-26","ACTUAL",{"date":37,"type":35},"2025-06-17",{"date":39,"type":21},"2026-12",{"name":41,"class":42},"Creo Medical Limited","INDUSTRY",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":54,"conditions":55,"keywords":56,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":63,"locationsCount":5},"100582885","bronchoscopic-microwave-ablation-of-lung-tissue-in-surgical-candidates---uk-100582885","NCT06869122","Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates - UK","Assessment of the Safety and Performance of the AB1 Electrosurgical System for Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates - UK","AB1MALTISC-UK","Inclusion Criteria:\n\nPatients who:\n\n1. Have signed informed consent.\n2. Subject is willing and able to comply with all aspects of the treatment and evaluation schedule.\n3. Are ≥ 18 years old.\n4. Have lung lesion(s)\u002Fnodule(s) which are histopathological confirmed as cancer.\n5. Have soft tissue lung lesion(s):\n\n   * ≤ 20 mm in the largest dimension of the pulmonary window\n6. Are candidates for surgical resection as determined by a multi-disciplinary team (MDT) or tumour board.\n7. \\> 10 mm of tumour-free lung parenchyma between target tumour and pleura or fissure.\n8. Subject is willing and able to comply with the study protocol requirements.\n9. Are assigned an ASA (American Society of Anaesthesiologists) score of ≤ 3 or the patient is deemed fit for general anaesthesia.\n\nExclusion Criteria:\n\nPatients who:\n\n1. Have target nodule(s) within the International Association for the Study of Lung Cancer (IASLC) \"Central Zone\" (including bronchial tree, major vessels, heart, oesophagus, spinal cord, and phrenic \\& laryngeal nerves).\n2. Are pregnant or breast feeding, as determined by standard site practices.\n3. Have participated in an investigational drug or device research study within 30 days of enrolment that would interfere with this study.\n4. Have a physical or psychological condition that would impair study participation or jeopardise the safety or welfare of the subject.\n5. Have an expected survival less than 12 months.\n6. Have an implantable device, including pacemakers or other electronic implants.\n7. Have known pulmonary hypertension (PASP \\[pulmonary artery systolic pressure\\] \\>50mmHg).\n8. Subject had a prior pneumonectomy.\n9. Diagnosis of Small Cell Lung Cancer.\n10. Subject had a therapeutic intervention (e.g., SBRT) within same lobe as the target lesion.\n11. Subjects currently undergoing or underwent chemotherapy, systemic immunosuppressive treatment, or radiotherapy within 3 months of planned Study procedure.",{"count":53,"type":21},18,"This study involves the use of a medical device, the Creo Medical MicroBlate Flex instrument, to heat and destroy lung tumour cells using microwave energy (this is also called ablation). In this study, the investigators are investigating whether the ablation instrument can be used effectively to treat lung tumours or tumours that have spread to the lungs. If successful, using this technology may mean future patients may not need to undergo surgical removal of these types of lung tumours.\n\nThe aim of this study is to evaluate the safety and performance of the MicroBlate Flex instrument in treating individuals with cancerous lung tumours that are due to be removed by surgery. All participants in the study will undergo the microwave ablation procedure, which is a separate and additional procedure to their surgical procedure.\n\nThe study, funded by Creo Medical, will be conducted at sites in the UK and Italy, and will involve up to 18 participants.",[25],[27,28,29,30],"2026-04-16",{"date":59,"type":35},"2026-04-21",{"date":61,"type":35},"2025-07-14",{"date":39,"type":21},{"name":41,"class":42},""]