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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | CT-guided percutaneous radiofrequency ablation | Percutaneous 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.