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NCT01454271
Follow up Study of Patients Undergoing Total Hip Arthroplasty CERAFIT® Grafted With Poly Sodium Styrene Sulfonate
Phase 1, PHASE2 trial testing Total Hip Arthroplasty Replacement in Hip Arthroplasty Replacement. Withdrawn.
Quick facts
| Lead sponsor | Societe ACTIVBIOMAT |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Withdrawn |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | prevention |
| Sites | 1 location across France |
Drugs / interventions tested
- Total Hip Arthroplasty Replacement
Conditions studied
- Hip Arthroplasty Replacement — all drugs for Hip Arthroplasty Replacement →
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.
Verify or expand the search:
- PubMed search for NCT01454271
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Hip Arthroplasty Replacement
Currently open trials in the same condition.
- NCT07392515 — Cognitive and Physical Recovery After Hip Fracture in Frail Patients Using Digital Rehabilitation Technology · NA · recruiting
- NCT07110324 — Characteristics of Persistent Pain Composition Following Total Hip or Knee Arthroplasty: a Descriptive Study · 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 NCT01454271 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Societe ACTIVBIOMAT
- Last refreshed: 14 August 2018
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