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NCT03451149 · ClinicalTrials.gov registry record · NA

Feasibility And Safety Of Transjugular Intrahepatic Portosystemic Shunt (TIPS) Creation Using A Radiofrequency Guidewire

A NA study, sponsored by Oregon Health and Science University.

Completed
Registry status
NA
Development phase
10
Enrollment target

NCT03451149 is a NA study that has completed, run by Oregon Health and Science University. The registered enrollment target is 10 participants.

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The verdict

NCT03451149, a NA study, has completed, sponsored by Oregon Health and Science University.

COMPLETED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

A novel radiofrequency (RF) wire created by Baylis Medical (Montreal, CAN) is an FDA cleared device commonly used for percutaneous recanalization procedures. This wire has an active tip that delivers focused RF energy and has been applied for many procedures such as percutaneous transseptal left heart access, recanalization of central vein occlusion, recanalization of arterial occlusion, and recanalization of bile duct occlusion. There has been no study investigating the use of the RF wire for TIPS creation in clinical practice with humans. Having promising results of an experimental feasibility investigation in swine, the investigators are seeking to assess the feasibility and safety of the RF wire to cut through tissue in the liver while creating TIPS in the clinical setting.

Interventions

  • DEVICE Radiofrequency wire (Powerwire)

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2017-10-25
Est. Completion 2019-01-29
Phase NA

What the Registry Record Tells You About NCT03451149

The ClinicalTrials.gov registry entry for NCT03451149 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Oregon Health and Science University, which has 546 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Radiofrequency wire (Powerwire) is the first listed.

NCT03451149 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03451149 about?

NCT03451149 is a clinical study titled "Feasibility And Safety Of Transjugular Intrahepatic Portosystemic Shunt (TIPS) Creation Using A Radiofrequency Guidewire". A novel radiofrequency (RF) wire created by Baylis Medical (Montreal, CAN) is an FDA cleared device commonly used for percutaneous recanalization procedures. This wire has an active tip that delivers focused RF energy and has been applied for many procedures such as percutaneous transseptal left hea...

What is the current status of trial NCT03451149?

This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2017-10-25. Estimated completion is 2019-01-29.

What interventions are being tested in trial NCT03451149?

The interventions under investigation include: Radiofrequency wire (Powerwire) (DEVICE).

Who is sponsoring clinical trial NCT03451149?

This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.

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

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.