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Clinical Trials/NCT05477251
NCT05477251Not yet recruitingNot Applicable

Comparative Study on the Efficacy and Safety of Microwave Ablation and Lobectomy in the Treatment of Ground Glass Nodules Located in the Pulmonary Hilar Region

RenJi Hospital0 sites100 target enrollmentStarted: October 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
100
Primary Endpoint
3-year recurrence-free survival rate

Study Overview

Brief Summary

GGO is a characteristic focus of early lung cancer. Due to the abundant peripheral blood vessels and bronchial tissues around the GGO lesions located in pulmonary hilar, only lobectomy could be used for the surgical treat of hilar GGO lesions which will make the significantly decline of the pulmonary function after surgery and affect the quality of life to a great extent. Our previous study has reported a new blunt-tip MWA electrode (MTC-3CA-II3, Vison Medical Inc.) for the treatment of GGO lesions. The blunt-tip MWA electrode could improve the safety of GGO ablation, significantly reduce the occurrence of bleeding and hemoptysis, which made it possible to ablate GGO in the hilar region safely. In this study, the blunt-tip MWA electrode was used in the treatment of patients with hilar GGO lesions, and the efficacy and safety of microwave ablation and lobectomy in the treatment of ground glass nodules located in the pulmonary hilar region were evaluated and compared.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •The age ranged from 18 to 75 years old, male or female;
  • •GGO lesions in the hilar region were diagnosed by imaging examination (CT / PET-CT). During the follow-up of 6-12 months, the lesions increased by more than 2mm, the solid components increased, or there were obvious solid components, or the GGOs were judged to be highly malignant by imaging.
  • •The size of GGO lesions was 8mm-3cm, and the number of nodules was ≤
  • •There was no lymph node metastasis, intrapulmonary metastasis or distant organ metastasis;
  • •After multidisciplinary evaluation, the patients were feasible for lobectomy and CT guided microwave treatment;
  • •No bleeding tendency, normal coagulation function or coagulation dysfunction can be corrected after treatment;
  • •Patients and /or family members agreed to join the clinical trial and signed informed consent.

Exclusion Criteria

  • •The general condition of the patient is very poor, ECOG physical fitness score > 2, unable to tolerate lobectomy and MWA treatment, or has relevant contraindications;
  • •The lesions had received other treatments before; patients with regional lymph node metastasis or distant metastasis or with pleural fluid and ascites;
  • •Patients with poor compliance;
  • •Severe heart, lung, kidney, brain and other important organ diseases;
  • •The researcher believes that it is not suitable for inclusion

Arms & Interventions

microwave ablation

Experimental

Intervention: microwave ablation (Procedure)

lobectomy

Active Comparator

Intervention: lobectomy (Procedure)

Outcomes

Primary Outcomes

3-year recurrence-free survival rate

Time Frame: 3 year after treatment

3-year recurrence-free survival rate

Secondary Outcomes

  • Postoperative hospital stay(During hospitalization)
  • Total hospitalization expenses Total hospitalization expenses(During hospitalization)
  • Incidence of complications(Within 1 month after operation)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chi Jiachang

Deputy Chief Physician

RenJi Hospital

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