Post-marketing Surveillance Study of the Saphir Stem in Primary Hip Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGruppo Bioimpianti S.r.l.

About this trial

Post-market clinical follow up investigation on the use of saphir stem and FIN Cup or Dualis system in the treatment of pathologies requiring hip arthroplasty. The main object of the clinical investigation is the evaluation of long term survival rate of Saphir stem.

Eligibility criteria

Qualifiers

patients>18 years

Candidate for primary total hip replacement with femoral stem and acetabular cup

if ostheoarthritis patients aged 18 to 85 years

if femoral neck fracture patients aged 18 to 90 years

Disqualifiers

<18 years

if female, pregnant

patient who has already had primary hip surgery on the same side

local or disseminated neoplastic disease

Trial design

Treatments tested in this trial

  • hip arthroplasty with prosthesis

Treatment groups

No treatment groups listed

Sponsors and collaborators