Freezing lung nodules: a new alternative to surgery?
NCT ID NCT06848881
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two treatments for small lung spots called ground-glass nodules: cryoablation (freezing the nodule) and thoracoscopic surgery (removing it). Researchers want to see which approach is safer and better at preventing the nodules from coming back. About 160 adults with nodules 8-20mm in size will take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cryoablation (freezing procedure) and thoracoscopic surgery
- What this could lead to
- If cryoablation works as well as surgery, it could offer a less invasive option for treating early lung nodules, with faster recovery and fewer complications.
- What could go wrong
- This is a relatively small, early-stage study (160 people). Cryoablation may not be as effective as surgery at preventing cancer from coming back, and there could be unknown risks.
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
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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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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2025
- Expected to finish
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Apr 2030
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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients ≥ 18 years old. 2. The size of the GGN is 8-20mm (with less than 25% solid component), and the number of nodules requiring treatment in the short term is less than 3. 3. Pathological confirmation of the GGN as non-small cell lung cancer; or progression of the GGN during at least 3 months of follow-up, including enlargement of the largest diameter, increase in solid component, or the appearance of a significant solid component in a previously pure GGN, with multidisciplinary discussion (including radiology, thoracic surgery, and pulmonology) suggesting malignancy. 4. No lymph node, pulmonary, or distant metastasis to other organs. 5. After multidisciplinary evaluation, the patient is considered capable of tolerating both surgical and ablation procedures. 6. Unsuitable for radiation therapy or refusal of radiation therapy. 7. Willing to participate in this clinical study and sign the informed consent form. Exclusion Criteria: 1. Patients in poor general condition, with ECOG physical fitness score \>2, unable to tolerate surgery or ablation therapy, or with relevant contraindications. 2. Patients who have previously received other treatments for pulmonary GGNs. 3. Patients with poor compliance. 4. Severe heart, lung, kidney, brain, or other vital organ diseases. 5. Active bacterial or fungal infections. 6. Simultaneous or metachronous (within the past 5 years) double cancers. 7. Women during pregnancy or breast-feeding. 8. History of radiation therapy. 9. Bleeding tendency, abnormal coagulation functions, or coagulation disorders that cannot be corrected after treatment. 10. Contraindications to general anesthesia. 11. Expected survival time \< 6 months. 12. The researcher believes that it is not suitable for inclusion.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine
RECRUITINGShanghai, Shanghai Municipality, China
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