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Prosthesis Survival clinical trials

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NCT ID: NCT04960098 Recruiting - Knee Osteoarthritis Clinical Trials

Patient-reported Outcome Measures in Patient Underwent Total Hip and Knee Arthroplasty

Start date: January 12, 2016
Phase:
Study type: Observational [Patient Registry]

Registry of Galeazzi Orthopedic Institute: provides for the regular and systematic collection of all data (clinical and some PROMs) obtained from patients undergoing hip and knee arthroplasty to which questionnaires are proposed investigating the specific functional sphere of the joints undergoing surgery (Knee injuryOsteoarthritisOutcomeScore (KOOS-PS) and Hip injuryOsteoarthritisOutcomeScore (HOOS-PS) but also the sphere of general health (ShortForm health survey-12 (SF-12) and VisualAnalogueScale (VAS)) , in addition, of course, to the satisfaction rate.

NCT ID: NCT04773873 Completed - Prosthesis Survival Clinical Trials

Implant Retained CAD-CAM Ceramic Crowns

RCT-Scherrer
Start date: January 1, 2015
Phase: N/A
Study type: Interventional

Newly available ceramic CAD-CAM blocs containing a screw channel for chairside-made crowns to be adhesively cemented to a TiBase abutment and screw-retained to an implant are appealing to the clinician, considering the time efficiency (one appointment) and overall lower costs as no dental laboratory is involved. The hypotheses are that the biological (BOP, PD, PCR, implant bone level) and mechanical outcomes (fracture, loss of retention, wear) are equivalent to implant screw-retained Porcelain-Fused-to-Metal (PFM) crowns over a 5 year observation time.This RCT will provide key information as to the cost/benefit, suitability and/or limitations of these chair-side hybrid-abutment crowns in the posterior region.

NCT ID: NCT04748458 Completed - Prosthesis Survival Clinical Trials

Long-term Outcomes of Conical Tapered Stems in Cementless Total Hip Arthroplasty Due to Congenital Hip Pathologies

RetroCone
Start date: July 17, 2020
Phase:
Study type: Observational

A retrospective consecutive population of patients treated with conical tapered stems in cementless total hip arthroplasty for osteoarthritis due to congenital hip pathologies will be selected. The aim of this retrospective study is to evaluate the long-term clinical and radiographic results of this implant and the survival rates in such a specific cohort.

NCT ID: NCT04688593 Recruiting - Osteoarthritis, Hip Clinical Trials

Clinical and Functional Outcome of the MobileLink Acetabular Cup System in the Short-, Mid-, and Longterm Follow-up

Start date: May 4, 2021
Phase:
Study type: Observational

The implantation of artificial hip joints is one of the most frequently performed surgeries. Normally, patients are very satisfied with the results. The MobileLink hip prosthesis system is a CE marked medical device. This means the the safety and performance of the prosthesis ist approved. Aim of the study is to collect clinical data about the outcome of the MobileLink hip prosthesis system under routine condition and to determine the satisfaction of the patients.

NCT ID: NCT04446078 Completed - Dental Implants Clinical Trials

Hybrid Polyetheretherketone (PEEK)-Acrylic Resin Prostheses and the All-on-4 Concept for Full Arch Rehabilitation

AO4PEEKDev
Start date: May 2, 2014
Phase: N/A
Study type: Interventional

It is necessary to evaluate the outcome of implant supported fixed prosthetic rehabilitations using peek material. To test this, the study design to be used will be a prospective single cohort to evaluate the long term outcome of fixed prosthetic implant supported rehabilitations. The cohort will be evaluated after 5 years of follow-up, regarding prosthetic survival, implant survival, marginal bone resorption, incidence of mechanical complications (loosening or fracture of prosthetic components), biological complications (peri-implant pathology, suppuration, fistulae), incidence of biological complications (peri-implant pathology, suppuration, excessive marginal bone resorption) in-mouth comfort, overall chewing feeling, framework integrity, veneer adhesion, veneer chipping, patient tissue reaction, denture staining, manufacture issues,

NCT ID: NCT04374201 Active, not recruiting - Prosthesis Survival Clinical Trials

14y Prospective Study on Posterior Zirconia-based 3-unit FDPs

Start date: November 1, 2004
Phase:
Study type: Observational

The main objective of the present prospective study is to evaluate the effectiveness of posterior zirconia FDPs after 14 years of function.

NCT ID: NCT04244929 Completed - Prosthesis Survival Clinical Trials

Multicenter Perspective Study: Clinical Evaluation of the Persona MC® With Preservation or Sacrifice of the PCL

Start date: December 20, 2019
Phase: N/A
Study type: Interventional

Prospective, multicenter study on the Total Knee Prosthesis available on the market "Persona Medial Congruent® knee". Primary endpoint -Evaluation of the survival of the implant after 5 years of follow-up Secondary endpoints - Evaluation of the survival of the implant at 10 years of follow up. - Evaluation of clinical and radiographic outcomes in Italian patients undergoing total knee replacement with the Persona Medial Congruent® implant with sacrifice or retention of the posterior cruciate ligament (PCL)

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)?

NCT ID: NCT02931903 Completed - Prosthesis Survival Clinical Trials

Lithium Disilicate Glass-ceramic Versus Hybrid Ceramic Superstructure Materials on Implant Stability

RCT
Start date: January 2017
Phase: N/A
Study type: Interventional

The aim of this study is to assess the effect of the newly introduced (hybrid dental ceramic) superstructure materials, Vita Enamic versus IPS Emax on implant stability, patient satisfaction and crestal bone loss.