About this trial
Thermal ablation is an established treatment for lung cancer. It involves insertion of a applicator under image guidance into a lung tumour and destroying it with radiofrequency, microwave or cryotherapy. One of the common side effects is pneumothorax, which is a leak of gas from the lungs when it punctured. Air leak necessitates placement of a drainage tube in more than half of patients undergoing the procedure. The drain can be associated with some morbidity including pain, reduced mobility, prolonged hospital stay and infection Pleural embolization refers to the injection of substances to the linings of the lung to seal air leakage. There is published evidence in using pleural embolization with autologous blood (blood drawn up from the patient's veins) to prevent pneumothorax in patients undergoing lung biopsies. This technique is also known as pleural blood patch (PBP). A study involving more than 4000 patients found that PBP reduced the rates of pneumothorax by 35% and drain placement by 55% in lung patients. A study using prophylactic gelfoam torpedo embolization for radiofrequency ablation showed significant reduction in chest drain rates.
In this study, investigators plan to evaluate the PBP using a tandem needle technique in patients undergoing lung ablation at the Oxford Thermal Ablation Service, one of the largest units in the country performing about 200 ablations per year, mostly microwave ablations. Patients will be randomized to receive lung ablation with or without the PBP.
The PBP technique is easy to learn, enjoys high technical success rates and does not expose the patient to any significant additional risk.
The primary outcome is the chest drains rates in the two trial groups:
1. patients undergoing lung ablation without PBP and 2. patients undergoing lung ablation with PBP. Other outcomes that would be measured include the volume of gas leakage on Computed Tomography (CT) imaging, safety profile, length of stay, feasibility of same day discharge, patient oriented outcomes including validated pain score, and institution oriented outcomes including medical costs.
A positive trial could significantly reduce the side effect profile of lung ablation and hasten the patient's recovery. There could be significant savings in healthcare costs as the procedure may become safe to perform as a day procedure as opposed to an overnight procedure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Clinically indicated for lung ablation.
Willing and capable of giving informed consent.
Aged 18 years or above.
Disqualifiers
Unable to proceed to lung ablation procedure.
3 or more lung lesions to be ablated in the same setting.
Trial design
Parallel
Treatments tested in this trial
Pleural embolisation
Procedure/SurgeryAdministration of pleural blood patch with tandem needle technique
Treatment groups
Trial outcomes
Primary outcomes
Perioperative chest drain insertion
To compare the rates of clinically important pneumothorax in patients undergoing lung ablation with or without pleural blood patch embolisation Chest drain rates (%) are expressed in means and standard deviations.
Secondary outcomes
Pneumothorax volume on immediate post ablation CT imaging
To evaluate the difference in volume of pneumothorax between intervention and control group Pneumothorax volume (mL) are expressed in means and standard deviations.
Technical success in interventional group
To evaluate the technical success rate of the intervention in concern Technical success rate (%) is only for interventional group and expressed in a descriptive percentage.
Adverse events deemed due to PBP
To evaluate the safety of pleural blood patch embolisation Adverse event is quantified by CIRSE system (1-6), an ordinal scale variable.
Pain score
To evaluate the patient tolerance between intervention and control group Measured by visual analogue scale 1-10 ( interval scale variable, expressed in means and standard deviations)
Sponsors and contacts
Click on the lead sponsor to view all of their trials.