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Clinical Trial ● Currently Recruiting NCT06869122

Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates – UK

Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates – UK — Recruiting • Oncology • NCT06869122.

📅 21 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT06869122
Sponsor
Creo Medical Limited
Start
2025-07-14
ClinicaliQ Trial Snapshot
  • Bronchoscopic Microwave Ablation of Lung Tissue in Surgical Candidates – UK — Recruiting • Oncology • NCT06869122.
  • Sponsor: Creo Medical Limited.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
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.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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