Evaluation of Safety and Feasibility of EUS-guided RFA for Solid Pancreatic Neoplasms
Pancreatic Cancer, Pancreatic Neoplasms, Pancreatic Adenocarcinoma
About this trial
This is an interventional treatment trial for Pancreatic Cancer focused on measuring EUS-guided RFA, Endoscopic ultrasound, radio frequency ablation
Eligibility Criteria
Inclusion Criteria:
- Age 21 years-old or above
- Suffering from pancreatic neuroendocrine tumour or pancreatic ductal carcinoma that was confirmed by fine needle aspiration cytology
Unsuitable for surgery, due to one (or more) of the following items:
- ASA score >/= III
- An alternative advanced malignancy
- Unsuitable for surgery upon expert's opinion for any other reason
- Individuals who are not keen for surgical resection
- Eligible for endoscopic intervention
- Written informed consent
Exclusion Criteria:
- Coagulopathy (international normalized ratio >1.5, partial thromboplastin time greater than twice that of control), platelet count <50,000x103/uL
- Pregnancy
- Patients with a poor mental condition or mental retardation, unable to understand the nature and possible consequences of the study
- Patients unwilling to undergo follow-up assessments
- Patients with liver cirrhosis, portal hypertension and/or gastric varices.
Sites / Locations
- Singapore General Hospital
Arms of the Study
Arm 1
Experimental
EUSRA RFA needle
This procedure is very similar to the standard technique of EUS-guided fine needle aspiration. All patients would undergo EUS with a linear array or therapeutic echoendoscope. The location and size of the lesion would be assessed for suitability of treatment. After locating the lesion, the EUSRA RFA needle would be inserted to the centre of the lesion. RFA would then be initiated and hyperechoic interferences would be observed around the electrode signifying heating of the tissue.