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Clinical Trials/NCT02629978
NCT02629978
Unknown
Not Applicable

Efficacy and Safety of Radiofrequency Ablation of Malignant Pulmonary Nodules

Chinese PLA General Hospital1 site in 1 country500 target enrollmentOctober 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Chinese PLA General Hospital
Enrollment
500
Locations
1
Primary Endpoint
complication rate
Last Updated
10 years ago

Overview

Brief Summary

The objective of this study is to evaluate the outcomes of radiofrequency ablation in the treatment of patients with malignant pulmonary nodules(not exceed 3cm )who are not suitable candidates for or refuse surgical resection.

Detailed Description

Percutaneous radiofrequency ablation (RFA) is a minimally invasive technique widely used to treat solid tumors. Patients with malignant pulmonary nodules will undergo a series of CT- guided percutaneous RFA procedures. During the procedures,percutaneous needles will be inserted into the target tissues under CT guidance,the needles deliver thermal energy and then destroy the tumors by causing coagulation necrosis via tissue heating. The purpose of this study is to assess the effectiveness and safety of RFA in pulmonary nodules (maximum tumor diameter ≦30 mm) was 10 mm apart from the big trachea, primary bronchi, esophagus, great vessels,heart and pleura. Preoperative and postoperative evaluations,including recent laboratory tests evaluated and imaging studies reviewed,will be performed both before and after the procedures.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
October 2020
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Chinese PLA General Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yueyong Xiao

Director of the Department

Chinese PLA General Hospital

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed malignant pulmonary nodules.
  • Patients refuse or are not suitable for surgical resections.
  • 1-3 pulmonary nodules , with a maximum tumor diameter ≦30 mm.
  • Minimum distance of nodules are at least 10 mm apart from the surrounding tissues as big trachea, primary bronchi, esophagus, great vessels,heart and pleura.

Exclusion Criteria

  • Patients who has uncorrectable coagulation disorders, severe heart or pulmonary failure, or uncontrolled infections.
  • With extensive extrapulmonary or intrapulmonary metastasis.
  • Have taken anticoagulant as aspirin in one week.
  • Target nodules nearby pleura or other important hilum and mediastinum structures.
  • With metal implants are adjacent to the target tissues which will be covered with ablation area.

Outcomes

Primary Outcomes

complication rate

Time Frame: During the procedure or up to 5 years after the procedures

Including puncture-related complications such as pulmonary haemorrhage, hemothorax, pneumothorax, cardiac tamponade, and air embolism and ablation-related complications such as chest pain, pleural reactions, cough, and skin burns.

1- , 3- and 5-year survival rates

Time Frame: up to 5 years after the procedures

Secondary Outcomes

  • changes of the size about the tumor on CT/MRI images(After the procedures up to three months)

Study Sites (1)

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