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NCT01454271

Follow up Study of Patients Undergoing Total Hip Arthroplasty CERAFIT® Grafted With Poly Sodium Styrene Sulfonate

Withdrawn Phase 1, PHASE2 Last updated 14 August 2018
What this trial tests

Phase 1, PHASE2 trial testing Total Hip Arthroplasty Replacement in Hip Arthroplasty Replacement. Withdrawn.

Quick facts

Lead sponsorSociete ACTIVBIOMAT
PhasePhase 1, PHASE2
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Societe ACTIVBIOMAT

Who can join

Adults 18 to 75, any sex, with Hip Arthroplasty Replacement. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The risk of infection after primary Total Hip Arthroplasties (THA)is generally estimated to be less than 1% but remains a severe and costly complication, source of morbidity and even mortality. The "biofilm" forms very early after the bacterial contamination of the prosthesis and poses a number of clinical challenges due to his resistance to immune defence mechanisms and antibiotics. Preventive strategies are needed. The poly sodium styrene sulfonate (pNaSS) is a bioactive polymer. In vitro and in vivo studies showed that poly sodium styrene sulfonate grafted on titane surfaces reduce significantly the bacterial adhesion. They also proved his biocompatibility and osseous-integration.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Hip Arthroplasty Replacement

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/NCT01454271.

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