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Radio Frequency Ablation in the Management of Pancreatico-biliary Disorders: A Multicenter Registry

Radio Frequency Ablation in the Management of Pancreatico-biliary Disorders: A Multicenter Registry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01439698
Acronym
RFA-Registry
Enrollment
200
Registered
2011-09-23
Start date
2011-09-30
Completion date
2018-12-30
Last updated
2017-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bile Duct Cancer, Bile Duct Obstruction, Biliary Stricture, Cholangiocarcinoma, Pancreatic Cancer

Keywords

Cholangiocarcinoma, Pancreatic Cancer, Bile Duct Cancer, Biliary Stricture, Bile duct obstruction, ENDOHPB, Radio Frequency Ablation, RFA, ERCP, Endoscopic Retrograde Cholangiopancreatography, Registry, Multicenter

Brief summary

The objective of this protocol is to establish a multicenter registry to evaluate the impact of radiofrequency ablation in the management of patients with pancreatico-biliary disorders including malignancies.

Detailed description

Bile duct cancer and pancreatic cancer are cancers that cannot be surgically removed. As the cancer grows, it blocks the drainage of the bile ducts that carry digestive juices from the gall bladder and pancreas to the small intestine. ERCP (endoscopic retrograde cholangiopancreatography) is often prescribed during which a tube with a tiny camera attached is inserted through the subject's mouth and advanced to a place in the small intestine where the bile duct empties. Through this scope the doctor enlarges the ducts with tiny balloons and places plastic or metal stents (straws) that help keep the bile ducts open so they can drain properly. However, due to the cancer, the stents are blocked eventually. The purpose of this registry is to record information and evaluate the impact of radiofrequency ablation (RFA) of endoscopic radiofrequency ablation (RFA) probes in improving the management of bile duct cancer or pancreatic cancer by ablating the tissue in the bile duct(s) before the stent(s) are implanted. By using radiofrequency (RF) energy to heat the tissue in the duct(s) prior to stent(s) insertion, the surrounding tissue becomes coagulated and this may delay tumor growth and the time before the stent lumen becomes blocked. Thereby, allowing increased periods between the need for intervention and further stent implantation(s). The registry will evaluate the efficacy and safety of RFA procedures conducted for pancreatico-biliary disorders. The safety and efficacy of various radio frequency ablation probes have been assessed in a series of studies. This multi-center registry has been initiated: 1. To document the immediate and post procedure clinical performance of radio frequency ablation in a 'real world' patient population requiring stent implantation for pancreaticobiliary disorders. 2. To assess the immediate and 6 months post procedure adverse event rate in patients. 3. To assess the impact of RFA on the life expectancy of patients suffering from pancreaticobiliary malignancies.

Interventions

DEVICERadio Frequency ablation Probe

Any probe that can conduct radiofrequency ablation within biliary ducts.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who have undergone RFA for pancreaticobiliary disorders * Above 18 years of age

Exclusion criteria

* Patients who have not undergone RFA * Below 18 years of age

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Bile Duct Stricture Diameter.4 yearsEfficacy Assessment- Change from Baseline in Bile Duct Stricture Diameter.
Number of Participants with Adverse Events4 yearsSafety Assessment - Number of Participants with Adverse Events, type, frequency and intensity.

Secondary

MeasureTime frameDescription
Number of days of survival post intervention4 yearsDocumentation of response rates,overall survival duration and overall stent occlusion-free duration.
Number of overall stent occlusion-free days post intervention4 yearsDocumentation of overall stent occlusion-free duration post intervention to highlight quality of life and reduction of interventional procedures.

Countries

United States

Contacts

Primary ContactMichel Kahaleh, MD
mik9071@med.cornell.edu646-962-4000
Backup ContactMonica R Gaidhane, MD, MPH
mog2012@med.cornell.edu646-962-4796

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026