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NCT00479180

Safety of Vascugel Treatment After Creation of Arteriovenous Access for Hemodialysis Use

Completed Phase 1/Phase 2 Last updated 25 October 2011
What this trial tests

Phase 1/Phase 2 trial testing Vascugel in Hemodialysis Access in 65 participants. Completed in 1 June 2010.

Timeline
1 July 2006
Primary endpoint
1 June 2010
1 June 2010

Quick facts

Lead sponsorPervasis Therapeutics, Inc
PhasePhase 1/Phase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment65
Start date1 July 2006
Primary completion1 June 2010
Estimated completion1 June 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Pervasis Therapeutics, Inc — full company profile →

Who can join

Adults 18 to 89, any sex, with Hemodialysis Access. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

Vascugel™ is safe when placed at the anastomotic site at the time of surgery during creation of an AV graft or fistula for hemodialysis access.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Cell matrix contact modifies endothelial major histocompatibility complex class II expression in high-glucose environment.
    Nickmann M, Saemisch M, Wilbert-Lampen U, Nickel T, et al · · 2013 · cited 2× · PMID 24043258 · DOI 10.1152/ajpheart.00018.2013

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Other recruiting trials for Hemodialysis Access

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00479180.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing