ClinicaliQ Trial Snapshot
- Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates – UK — Recruiting • Oncology • NCT06869122.
- Device being tested: The Creo Medical MicroBlate Flex instrument delivers microwave energy via bronchoscopy to ablate (heat and destroy) lung tumour tissue in patients who are candidates for surgical resection.
- Patient eligibility overview: The study recruits surgical candidates with lung tumours suitable for resection, assessing whether bronchoscopic microwave ablation can be safely and effectively delivered as an alternative or complementary approach to conventional surgical management.
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- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
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What This Trial Is Studying
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. The aim of this study is to evaluate the safety and…
Eligibility Snapshot
- : Patients who: 1. Have signed informed consent.
- Subject is willing and able to comply with all aspects of the treatment and evaluation schedule. 3. Are ≥ 18 years old. 4. Have lung lesion(s)/nodule(s) which are histopathological confirmed as cancer. 5. Have soft tissue lung lesion(s): * ≤ 20 mm in the largest dimension of the pulmonary window 6. Are candidates for surgical resection as determined by a multi-disciplinary team (MDT) or tumour board. 7. > 10 mm of tumour-free lung parenchyma between target tumour and pleura or fissure.
- Subject is willing and able to comply with the study protocol requirements. 9. Are assigned an ASA (American Society of Anaesthesiologists) score of ≤ 3 or the patient is deemed fit for general anaesthesia.
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.