Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07232433

Safety and Efficacy Evaluation of Cryoablation in the Treatment of Ground-Glass Nodules

Led by Ruijin Hospital · Updated on 2026-01-22

90

Participants Needed

2

Research Sites

253 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lung cancer is the leading cause of cancer-related mortality worldwide, making early diagnosis and intervention critical. With the widespread adoption of low-dose computed tomography (LDCT) screening, the detection rate of pulmonary ground-glass nodules (GGNs) has increased significantly. Although video-assisted thoracoscopic surgery (VATS) remains the standard treatment for early-stage lung cancer, a considerable proportion of patients are ineligible for surgery due to advanced age, impaired cardiopulmonary function, or multiple nodules. Cryoablation, a minimally invasive ablation technique, uses ultra-low temperatures to induce tumor cell death. It offers distinct advantages, including well-defined ablation margins, reduced procedural pain, preservation of adjacent healthy structures, and potential immune activation, providing an important alternative for this patient population. However, the safety and long-term efficacy of cryoablation for GGNs require further high-quality clinical evidence. This study aims to conduct a prospective, single-center, open-label clinical trial to systematically evaluate the feasibility and outcomes of cryoablation (percutaneous or electromagnetic navigation bronchoscopy \[ENB\]-guided) for treating pulmonary GGNs. We plan to enroll 90 patients who meet the following criteria: pathologically or multidisciplinary team (MDT)-confirmed malignancy, GGN size ranging from 6-30 mm, solid component ratio \<25%, unsuitability for or refusal of surgery/radiotherapy, and an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. The primary endpoint is the 2-year local recurrence rate after ablation. Secondary endpoints include the 5-year local recurrence rate, 3- and 5-year disease-free survival (DFS) rates, technical success rate (ablation completion), perioperative complications (e.g., pneumothorax, hemorrhage, infection), postoperative pulmonary function, pain scores, length of hospital stay, and treatment-related costs. The results of this study will provide critical clinical evidence to support the use of cryoablation for GGNs, optimize patient selection criteria, and promote the advancement of this minimally invasive technique.

CONDITIONS

Official Title

Safety and Efficacy Evaluation of Cryoablation in the Treatment of Ground-Glass Nodules

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Malignancy confirmed by biopsy or multidisciplinary team (MDT) discussion
  • For a single ground-glass nodule (GGN), size between 6 and 30 mm
  • For multiple GGNs, each nodule sized 6 to 30 mm, with no more than 3 nodules needing treatment as agreed by MDT
  • Patient is ineligible for or refuses video-assisted thoracoscopic surgery (VATS)
  • Patient is ineligible for or declines radiotherapy or stereotactic body radiotherapy (SBRT)
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Patient shows good compliance and voluntarily consents to participate
Not Eligible

You will not qualify if you...

  • Severe heart, lung, liver, or kidney dysfunction making general anesthesia unsafe
  • Contraindications to bronchoscopy or CT-guided percutaneous puncture
  • High risk for percutaneous puncture for any target lesion or no feasible access route found by bronchoscopic planning
  • Platelet count less than 50 x 10^9/L or uncorrectable bleeding or coagulation disorders (prothrombin time over 18 seconds or prothrombin activity under 40%)
  • Participation in another interventional clinical trial or expected need for other antitumor treatments during this study
  • Any other condition the investigator judges makes the patient unsuitable for the trial

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China, 200025

Not Yet Recruiting

2

Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China, 200025

Actively Recruiting

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Research Team

H

Hecheng Li

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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