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NCT06572540Recruiting

Transthoracic vs Transbronchial Cryoablation for Early-stage Peripheral Lung Cancer

Transthoracic Versus Transbronchial Cryoablation for Early-stage Peripheral Lung Cancer: A Prospective, Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 18 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The study aims to compare the efficacy and safety of transthoracic cryoablation to transbronchial cryoablation in the treatment of early-stage peripheral lung cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
110 (estimated)
First submitted
20 Aug 2024
Start date
1 Sept 2024
Primary completion date
31 Dec 2025
Lead sponsor
Jiayuan Sun
Diseases
Lung cancer
NCT number
NCT06572540

What you commit to

  • Study type: Interventional
  • Planned participants: 110
  • From 1 Sept 2024 to the primary completion date, 31 Dec 2025
  • 5 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with severe pulmonary fibrosis and pulmonary arterial hypertension.
  • Infectious and radioactive inflammation around the lesion, skin infection at the puncture site that is not well controlled, systemic infection, high fever \>38.5°C.
  • Patients with severe hepatic, renal, cardiac, pulmonary and cerebral insufficiency, severe anaemia, dehydration and serious disorders of nutritional metabolism that cannot be corrected or improved in a short term.
  • Those with poorly controlled malignant pleural effusions.
  • Any other condition that the investigator considers inappropriate for participation in this study.

Lab values

  • Patients with platelets \<70×109/L, severe bleeding tendency and coagulation dysfunction that cannot be corrected in a short term.
  • Anticoagulation therapy and/or anti-platelet drugs (except dabigatran, rivaroxaban and other new oral anticoagulants) have not been discontinued more than 5\~7d before ablation.

Other

  • Eastern Cooperative Oncology Group (ECOG) score \>2.
  • Combination with other tumors with extensive metastases and an expected survival of \<6 months.
  • Patients with episodic psychosis.
  • Pregnant women, or patients with pregnancy plan during the study period.
  • Have participated or are participating in other clinical studies within 30 days.

Who the study is looking for

  • Age older than 18 years.
  • Primary peripheral lung cancer diagnosed by pathology and pre-procedure staging examination suggesting clinical stage T1N0M0, stage IA (including postoperative new and multiple primary).
  • The target lesion was evaluated to be feasible for both CT and bronchoscopy-guided ablation.
  • Patients who are not suitable for surgery or refuse surgery, agree to undergo initial ablation therapy and sign informed consent form.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (5)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
West China Hospital,Sichuan University
Coordinator of this site? Confirm its status
ChengduChinaNot yet recruiting
The First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaNot yet recruiting
Sir Run Run Shaw Hospital , affiliated with the Zhejiang University School of Medicine
Coordinator of this site? Confirm its status
HangzhouChinaNot yet recruiting
Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine,
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting
Henan Provincial People's Hospital
Coordinator of this site? Confirm its status
ZhengzhouChinaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.