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Prosthesis Failure clinical trials

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NCT ID: NCT03523364 Completed - Clinical trials for Survival, Prosthesis

Survival Rate of All Ceramic Restorations Treated With Air-Water-Blasting Protocol

Start date: January 5, 2017
Phase:
Study type: Observational

This study evaluates retrospectively the survival rate of all-ceramic restorations, cemented using AWB technique (test) compared to those cemented with conventional technique (control)

NCT ID: NCT03520101 Active, not recruiting - Clinical trials for Aortic Valve Stenosis

Comparison of the Balloon-Expandable Edwards Valve and Self-Expandable CoreValve Evolut R or Evolut PRO System for the Treatment of Small, Severely Dysfunctional Surgical Aortic Bioprotheses. The 'LYTEN' Trial

Start date: May 10, 2017
Phase: N/A
Study type: Interventional

The treatment with transcatheter aortic valve implantation (TAVI) of patients with small (≤23mm) surgical bioprostheses remains a challenge due to the increased transvalvular residual gradients and high rates of severe prosthesis-patient mismatch (PPM) following the procedure.

NCT ID: NCT03510065 Completed - Clinical trials for Survival, Prosthesis

Prevision® PMCF Study

Start date: January 1, 2016
Phase:
Study type: Observational

Monocentric, non-interventional Post-Market Clinical Follow-Up (PMCF) Study on past implantations of the Prevision® prosthesis; the survival rate of the Prevision® prosthesis shall be evaluated and compared to literature results on comparable Revision stems.

NCT ID: NCT03469687 Completed - Hip Osteoarthritis Clinical Trials

Symax International Study

Start date: November 2, 2004
Phase: N/A
Study type: Interventional

The uncemented Symax hip stem is developed through optimization of the uncemented Omnifit hip stem. The Symax stem design combines an anatomical anteverted proximal geometry with a straight distal section. The proximal part is coated with a biomimetic hydroxyapatite (HA) coating for improved osseointegration to enhance load transfer and to minimize proximal bone loss. The distal part is treated with an anodization surface treatment in order to prevent distal bone apposition, which is expected to prevent distal loading and reduce proximal stress shielding. Aim of this study is to report mid-term clinical performance and evaluate whether the radiographic features are in line with the design principles of the Symax hip in an international clinical study with 5 years of follow-up.

NCT ID: NCT03411044 Completed - Clinical trials for Rheumatoid Arthritis

Fitmore Hip Stem PMCF Study: A Multi-centre, Non-comparative, Prospective Post-market Clinical Follow-up Study.

Start date: February 8, 2008
Phase:
Study type: Observational

A multi-centre, non-comparative, prospective post-market clinical follow-up study to obtain survival, clinical and radiographic outcomes data on the Zimmer Fitmore Hip Stem.

NCT ID: NCT03410940 Terminated - Clinical trials for Rheumatoid Arthritis

PMCF Study of the CLS Brevius Stem With Kinectiv Technology

Start date: January 7, 2011
Phase:
Study type: Observational

This study is a multi-center, prospective, non-controlled post-market surveillance study. The primary objective of this study is to confirm the safety and performance of the CLS Brevius stem with Kinectiv technology by obtaining implant survivorship and clinical outcomes data for the commercially available stem.

NCT ID: NCT03239509 Completed - Surgery Clinical Trials

15 Years Outcomes Following Bioprosthetic vs Mechanical Aortic Valve Replacement Between 50-65 Years

ANDALVALVE
Start date: January 2017
Phase:
Study type: Observational

Currently there is an increase in the use of bioprosthesis worldwide (> 70% according to national data of the Spanish Society of Thoracic and Cardiovascular Surgery). There is conflicting evidence regarding the long-term survival of patients aged 50-65 years with mechanical (M) or biological (B) aortic prostheses. General consensus of greater complications associated with the use of long-life anticoagulation in M and of reoperation in B. Similar survival with lower MACCE complications in bioprosthesis could reconsider their choice in patients aged 50-65 years, specially in the current TAVI era. The investigators are going to perform a multicentric retrospective observational study (Registry) about 15 year-outcomes Following Bioprosthetic vs Mechanical Isolated Aortic Valve Replacement for Aortic Stenosis in Patients Aged 50 to 65 Years in 5 Cardiovascular Surgery Centers in Andalousia (south Spain)

NCT ID: NCT03045536 Recruiting - Clinical trials for Survival, Prostheses

Evaluation of Partial and Total Femoral Replacement

EFeRe
Start date: January 1, 2016
Phase: N/A
Study type: Observational

Several surgical options for the reconstruction of massive bone defects have been described and include biologic methods with autografts and allografts, and the use of tumor endoprostheses (total femoral replacement, TFR). Several types of modular TFR are available, but nevertheless unpredictable outcomes and high complication rates have been described from most authors. The aim of the present study was to compare complication rates after TFR performed with modular total femur prosthesis MML (Fa. ESKA/Orthodynamics) in patients with and without malignant disease.

NCT ID: NCT03041597 Completed - Clinical trials for Implant Complication

Dental Implant Supported Removable Dental Prostheses

Start date: September 1, 2009
Phase: N/A
Study type: Interventional

To prospectively monitor the survival rate of Ankylos® dental implants, comparing delayed versus immediate loading, using abutments with the SynCone® concept for implant-supported detachable dental prosthesis (ISDDP) in the edentulous upper jaw.

NCT ID: NCT02941575 Not yet recruiting - Prosthesis Survival Clinical Trials

Patient Satisfaction and Peri-Implant Tissue Success of Hybrid Ceramic Versus E-Max Superstructures

Start date: December 2016
Phase: N/A
Study type: Interventional

In patients receiving implants in the esthetic zone, would the use of new Nano hybrid ceramic crown material (Crystal Ultra) improve esthetic patient satisfaction and peri-implant tissue success when compared with Lithium Disilicate crown (E-max)?