New study pits heat, cold, and knife against lung cancer
NCT ID NCT07272356
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares three standard treatments for lung tumors: surgery, targeted radiation (SBRT), and minimally invasive thermal ablation (using heat or cold to destroy tumors). About 68 adults with early-stage lung cancer or limited lung metastases will be followed for two years. Researchers will measure how well each treatment controls cancer, affects breathing, and impacts quality of life, aiming to guide personalized treatment decisions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Thermal ablation (microwave or cryoablation)
- What this could lead to
- If successful, this could help doctors choose the best treatment for each patient, balancing cancer control with preserving lung function and quality of life.
- What could go wrong
- This is a small, non-randomized study with only 68 participants, so results may not apply to everyone. The treatments are already standard, so no major breakthrough is expected.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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68 people
The number who actually took part.
- Started
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Nov 2022
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults (18 years or older) * Verified systemic therapy-naive biopsy-proven NSCLC, stages from Tis to T2; or oligometastatic peripheral (≤ 5 lesions) lung disease; * All lesions are ≤3 cm in size and accessible for surgery, ablation or SBRT; * No local nodal or distant metastatic disease on diagnostic imaging; * Documented agreement on the recommended curative treatment by a multidisciplinary team, including a pulmonologist, interventional radiologist, radiation therapist, thoracic surgeon, and oncologist; * Documented patient's agreement to receive the intended therapy and to participate in this study via a signed informed consent form. Exclusion Criteria: * Central lung tumors (\<2 cm from the main bronchi or hilum); * \>5 or diffuse lung lesions, or prior local treatment to the same lesion; * Major comorbidities, physical or social limitations precluding trial participation; * Contraindications to general anesthesia, inability to temporarily withdraw antiplatelet therapy, or evidence of severe coagulopathy.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Lithuanian University of Health Sciences Kaunas Clinics
Kaunas, 50161, Lithuania
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