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NCT01303159 · ClinicalTrials.gov registry record · NA

Endoscopic Bipolar Radiofrequency Probe (ENDOHPB) in the Management of Unresectable Bile Duct and Pancreatic Cancer

A NA study, sponsored by Weill Medical College of Cornell University.

Terminated
Registry status
NA
Development phase
29
Enrollment target

NCT01303159 is a NA study that was terminated before completion, run by Weill Medical College of Cornell University. The registered enrollment target is 29 participants.

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The verdict

NCT01303159, a NA study, was terminated before completion, sponsored by Weill Medical College of Cornell University.

TERMINATED
Registry status
NA
Development phase
29 participants
Enrollment target

Study Summary

The purpose of this study is to assess safety and ability of the endoscopic bipolar radiofrequency ablation (RFA) probe (ENDOHPB) to produce an improvement in the management of cancer of the bile duct or the pancreatic duct. By using radiofrequency (RF) energy to heat the tissue in the duct prior to insertion of the stent, the surrounding tissue becomes coagulated and this may delay tumour growth and the time before the stent lumen becomes blocked. Thereby, allowing increased periods between the need for intervention and further stent deployment. The study will look to see if the ENDOHPB is able to keep the stent open longer and perhaps decrease the number of invasive procedures for occluded (blocked) stents.

Interventions

  • DEVICE Endoscopic bipolar radiofrequency probe (ENDOHPB)

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2010-03
Est. Completion 2014-01-13
Phase NA

What the Registry Record Tells You About NCT01303159

The ClinicalTrials.gov registry entry for NCT01303159 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Endoscopic bipolar radiofrequency probe (ENDOHPB) is the first listed.

NCT01303159 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01303159 about?

NCT01303159 is a clinical study titled "Endoscopic Bipolar Radiofrequency Probe (ENDOHPB) in the Management of Unresectable Bile Duct and Pancreatic Cancer". The purpose of this study is to assess safety and ability of the endoscopic bipolar radiofrequency ablation (RFA) probe (ENDOHPB) to produce an improvement in the management of cancer of the bile duct or the pancreatic duct. By using radiofrequency (RF) energy to heat the tissue in the duct prior to...

What is the current status of trial NCT01303159?

This trial is currently terminated. It is a NA study. The enrollment target is 29 participants. The study started on 2010-03. Estimated completion is 2014-01-13.

What interventions are being tested in trial NCT01303159?

The interventions under investigation include: Endoscopic bipolar radiofrequency probe (ENDOHPB) (DEVICE).

Who is sponsoring clinical trial NCT01303159?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.