Last reviewed · How we verify
NCT00479180
Safety of Vascugel Treatment After Creation of Arteriovenous Access for Hemodialysis Use
Phase 1/Phase 2 trial testing Vascugel in Hemodialysis Access in 65 participants. Completed in 1 June 2010.
1 June 2010
Quick facts
| Lead sponsor | Pervasis Therapeutics, Inc |
|---|---|
| Phase | Phase 1/Phase 2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 65 |
| Start date | 1 July 2006 |
| Primary completion | 1 June 2010 |
| Estimated completion | 1 June 2010 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Vascugel — full drug profile →
- Placebo Comparator
Conditions studied
- Hemodialysis Access — all drugs for Hemodialysis Access →
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.
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Safety of vascugel
Time frame: 6 months followed by 2.5 year extension
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):
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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
Verify or expand the search:
- PubMed search for NCT00479180
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hemodialysis Access
Currently open trials in the same condition.
- NCT07372027 — Single-Needle Distal Return for Long-Term Arteriovenous Fistula Care · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00479180 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Pervasis Therapeutics, Inc
- Last refreshed: 25 October 2011
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