Clinical Trials Directory

Trials / Unknown

UnknownNCT02629978

Radiofrequency Ablation of Malignant Pulmonary Nodules

Efficacy and Safety of Radiofrequency Ablation of Malignant Pulmonary Nodules

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Chinese PLA General Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDURECT-guided percutaneous radiofrequency ablationPercutaneous radiofrequency ablation (RFA) is a minimally invasive technique will be performed in patients with malignant pulmonary nodules in this group. RFA kills the tumors by causing coagulation necrosis via tissue heating. The electrode delivers thermal energy will be inserted into the target tissues under the CT guidance to ensure the area of ablation should cover the targets and the lung tissues 0.5-1.0 cm around the tumors. Post-operative scan and laboratory test will be conducted in time.

Timeline

Start date
2015-10-01
Primary completion
2020-10-01
Completion
2020-10-01
First posted
2015-12-15
Last updated
2015-12-15

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02629978. Inclusion in this directory is not an endorsement.