Viewing Study NCT07034092


Ignite Creation Date: 2025-12-24 @ 3:31 PM
Ignite Modification Date: 2025-12-27 @ 2:26 AM
Study NCT ID: NCT07034092
Status: NOT_YET_RECRUITING
Last Update Posted: 2025-07-17
First Post: 2025-06-13
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: PATH-03 Paraguay Feasibility Study
Sponsor: Pathfinder Medical
Organization:

Study Overview

Official Title: Feasibility Study to Evaluate the Safety and Efficacy of the ePATH System for endoAVF Creation
Status: NOT_YET_RECRUITING
Status Verified Date: 2025-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this study is to evaluate the safety and effectiveness of the ePATH system in the creation of an endovascular AVF (endoAVF) in patients who require or will soon require hemodialysis and are eligible for a fistula.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
Pathfinder Medical OTHER The study is funded only by Pathfinder Medical and is not listed in any other databases. View