CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 54 enrolled
Drug / intervention
Venous Window Needle Guidedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01471041
NCT01471041Phase 3Completed

Vital Access Venous Window Needle Guide for Salvage of AV FistulaE (SAVE) Trial

Vital Access Corp.·interventional·Posted Nov 11, 2011·Updated Jun 3, 2016

In Brief

A Phase 3 clinical trial evaluating Venous Window Needle Guide for End Stage Renal Disease and 2 related conditions. Completed, enrolled 54 participants across 2 sites.

Detailed Summary

The SAVE Study will evaluate the safety and efficacy of the Venous Window Needle Guide in achieving access of a deep, un-cannulatable arteriovenous fistula to complete hemodialysis as prescribed.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedNov 11, 2011
Enrollment StartDec 1, 2011
Primary CompletionMar 1, 2013
Study CompletionJun 1, 2013
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 14.6 years ago

Interventions

Venous Window Needle Guidedevice

Subcutaneous, extravascular needle guide made of medical-grade titanium