Clinical Trials Logo

Clinical Trial Summary

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


Clinical Trial Description

thirty-seven patients needing to replace either premolars or molars were involved and 48 3-unit zirconia-based FDPs were fabricated. Patients included in the present clinical study met specific inclusion criteria and clinical procedures were standardized.

Frameworks with a 9 mm2 cross section of the connectors and 0.6 mm minimum thickness of the retainers were made by means of Computer Aided Design/Computer Assisted Manufacturing. A resin cement was used to lute the restorations. The patients were recalled after 6 and 12 months and then yearly up to a total follow-up of 14 years. The United States Public Health Service criteria were used in order to examine technical and esthetic outcomes. Success and survival rates ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04374201
Study type Observational
Source Federico II University
Contact
Status Active, not recruiting
Phase
Start date November 1, 2004
Completion date December 31, 2025

See also
  Status Clinical Trial Phase
Completed NCT03041597 - Dental Implant Supported Removable Dental Prostheses N/A
Enrolling by invitation NCT05589519 - Partial Implant-supported Rehabilitation Using PEEK N/A
Recruiting NCT05649085 - Evaluation of Single-unit Implant-supported Prostheses Survival Using CoCr Prosthetic Abutments: Prospective Observational Study
Active, not recruiting NCT05589493 - Hybrid PEEK-Acrylic Resin Prostheses and the All-on-4 Concept for Full-Arch Rehabilitation - Routine Group N/A
Recruiting NCT04688593 - Clinical and Functional Outcome of the MobileLink Acetabular Cup System in the Short-, Mid-, and Longterm Follow-up
Completed NCT04446078 - Hybrid Polyetheretherketone (PEEK)-Acrylic Resin Prostheses and the All-on-4 Concept for Full Arch Rehabilitation N/A
Active, not recruiting NCT05261204 - Transcatheter Aortic Valve Implantation Versus Standard Surgical Aortic Valve Operation
Active, not recruiting NCT06114069 - Prosthetic Management of All on Four Versus All on Six to Rehabilitate Completely Edentulous Maxillary Ridge Opposed by Natural Teeth N/A
Recruiting NCT02409186 - A Phase III Study of Nimotuzumab Plus Concurrent Chemoradiotherapy in Loco-regional Esophageal Squamous Cell Carcinoma Phase 3
Enrolling by invitation NCT05589545 - PEEK Prostheses in the All-on-4 Concept Using Zygomatic Implants for Full-arch Rehabilitation. N/A
Completed NCT04748458 - Long-term Outcomes of Conical Tapered Stems in Cementless Total Hip Arthroplasty Due to Congenital Hip Pathologies
Completed NCT02931903 - Lithium Disilicate Glass-ceramic Versus Hybrid Ceramic Superstructure Materials on Implant Stability N/A
Completed NCT01918124 - A Phase II Trial of Adjuvant Radiotherapy Combined With Chemotherapy for Patients With High-risk Endometrial Cancer Phase 2
Recruiting NCT04960098 - Patient-reported Outcome Measures in Patient Underwent Total Hip and Knee Arthroplasty
Completed NCT04773873 - Implant Retained CAD-CAM Ceramic Crowns N/A
Not yet recruiting NCT02941575 - Patient Satisfaction and Peri-Implant Tissue Success of Hybrid Ceramic Versus E-Max Superstructures N/A
Completed NCT00374946 - A Clinical Evaluation of Wear Couples in THA N/A
Completed NCT04244929 - Multicenter Perspective Study: Clinical Evaluation of the Persona MC® With Preservation or Sacrifice of the PCL N/A
Enrolling by invitation NCT05589506 - Partial Rehabilitation Using a PEEK-acrylic Resin Removable Partial Denture N/A
Enrolling by invitation NCT05589532 - Single Tooth Implant-supported Fixed Prosthetic Rehabilitation Using PEEK. N/A