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NCT Number: NCT03218345

EUS-guided RFA for Pancreatic Neoplasms

Radiofrequency ablation has been used for treatment of solid neoplasms of the liver, lung, kidney and adrenal. Recently, EUS-guided RFA has become available and the device allows EUS-guided treatment of pancreatic neoplasms. The procedure has been shown to be feasible in the porcine pancreas and was used to treat small groups of patients that are not suitable for surgery suffering from pancreatic neoplasms.

The aim of the current study is to perform a multi-center prospective study on EUS-guided radiofrequency ablation (RFA) of solid pancreatic neoplasms. The hypothesis is that EUS-guided RFA is safe, feasible and effective for treating solid pancreatic neoplasms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Surgery, Prince of Wales Hospital

Hong Kong

Location status: Recruiting

Location contact

Anthony YB Teoh

PRINCIPAL_INVESTIGATOR

Anthony YB Teoh, FRCSEd(Gen)

CONTACT

[email protected]

85226322953

About this study

RFA causes tissue destruction through the application of a high frequency alternating current, generating local temperatures above 60°C and leading to coagulative necrosis. The technique has been widely used in many solid organ tumors and has been shown to result in 5-year survival rates comparable to surgery. The technique is currently the standard therapy in hepatocellular carcinoma and colorectal pulmonary metastasis particular in patients that are not suitable for surgery.

This study is a multi-center prospective study involving four high volume international institutions. Consecutive patients suffering from pancreatic neuroendocrine tumors and pancreatic cancers would be recruited. EUS-guided RFA would be performed using a 19-gauge RFA electrode and a generator. The primary outcome would be the overall adverse events rate. Secondary outcomes include mortality, technical success rate, completion ablation rate, 1 & 3 year overall and disease-free survival.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years-old or above
  • Suffering from pancreatic neuroendocrine tumor or pancreatic ductal carcinoma (<5cm in largest diameter) that was confirmed by fine needle aspiration cytology
  • Unsuitable for surgery, due to one (or more) of the following items:
  • ASA score > II*
  • An alternative advanced malignancy
  • Unsuitable for surgery upon expert's opinion for any other reason
  • Healthy individuals who are not keen for surgical resection
  • Eligible for endoscopic intervention
  • Written informed consent

Exclusion criteria

  • Coagulopathy (international normalized ratio >1.3, 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.

Treatment and study plan

EUS-guided RFA

Procedure

EUS-guided RFA would be performed using a 19-gauge RFA electrode and a generator

Primary outcomes

  1. Severe adverse events

    Time frame: 30 days

    Adverse events specific to RFA would be graded according to the lexicon of endoscopic adverse events 24. Potential adverse events specific to RFA include: post-RFA syndrome, pancreatitis, pancreatic leak, thermal injury

Secondary outcomes

  1. Technical success rates

    Time frame: 1 week

    defined as successful puncture of the lesion with the RFA needle and completion of the ablation cycle.

  2. Procedural times

    Time frame: 1 day

    Duration of the procedure

  3. Hospital stay

    Time frame: 30 days

    Duration of hospital stay

  4. Radiological response

    Time frame: 1 year

    Based on modified RECIST criterion

  5. Number of re-interventions

    Time frame: 1 year

    Number of re-interventions after the procedure

  6. Survival

    Time frame: 3 years

    Duration of survival after the procedure

Study contacts

Contact information is provided by the study sponsor or research team.

Anthony YB Teoh, Professor

CONTACT

[email protected]

26322956

Sponsors and collaborators

Lead sponsor

Chinese University of Hong Kong

Other

Registry information

Official study title

Multi-center Prospective Study on EUS-guided Radiofrequency Ablation for Solid Pancreatic Neoplasms

Important dates

Study start
2016
Primary completion
2027
Study completion
2027
First posted
Jul 14, 2017
Registry last updated
Mar 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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