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Partially Edentulous Mandible clinical trials

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NCT ID: NCT06460103 Not yet recruiting - Clinical trials for Partially Edentulous Mandible

Peri-implant Bone Formation of Grafted Sites Around Hydrophilic and Non-hydrophilic Dental Implants

Start date: July 2024
Phase: N/A
Study type: Interventional

Although bone grafting at the same time as the placement of dental implants is a common procedure in implantology, there are currently no data on the influence of different types of implant surfaces on bone healing, which is crucial for implant stability. The primary objective of this study is to assess if implant surface properties, i.e. hydrophilicity, affect the osseointegration of the implant in simultaneously augmented bone. The secondary objective is to assess if implant surface properties, i.e. surface hydrophilicity, may affect the quantity of newly formed bone in the implant in simultaneously augmented bone. Surface hydrophilicity modification is a well-adapted concept in dental implantology and is clinically well-established. In this prospective study, all participants will receive a bone graft after extraction. After randomization, one group will receive a provisional SLA surface implant and another group will receive a provisional SLActive surface implant. The same standard surgical procedure will be performed for both groups when the definitive implant will be placed. The study will run for a total of 3 year, and 35 patients per group will be included. The Straumann SLA and SLActive implants, Maxgraft allograft and collprotect collagen membranes used in this study are all approved products on the Swiss market.

NCT ID: NCT05983718 Recruiting - Dental Implantation Clinical Trials

A Study of Surgical Guide Assisted Dental Implantation in Bangladesh

Start date: August 23, 2023
Phase: N/A
Study type: Interventional

This is a randomized controlled study that aims to compare the accuracy between full-guided with guide-pin-assisted free-hand dental implant surgeries. The basis of evaluation in each case is the comparison of the preoperative digital plan with the actual postoperative status.

NCT ID: NCT05079048 Completed - Clinical trials for Partially Edentulous Mandible

PEEK Retentive Elements Versus Conventional

PEEK
Start date: July 1, 2017
Phase: N/A
Study type: Interventional

comparing retention and patient satisfaction of implant-supported mandibular overdentures retained by conventional nylon clip and metal housings for ball attachments versus PEEK clip and housings

NCT ID: NCT05016401 Completed - Tooth Loss Clinical Trials

Performance and Safety of Use of the "KONTACT PERIO LEVEL" Transgingival Titanium Dental Implant

KPL
Start date: November 6, 2020
Phase:
Study type: Observational

As part of post-marketing clinical follow-up, BIOTECH DENTAL sets up the collection and evaluation of clinical data proactively with the aim of confirming the safety, performance as well as the constantly acceptable nature of the risks identified and of detecting potential emerging risks with the use of "Kontact Perio Level" implants in everyday practice.

NCT ID: NCT03814655 Completed - Clinical trials for Partially Edentulous Mandible

Evaluation of the Accuracy of Full Digital Workflow for Guided Implant Surgery Using the R2 Gate Software

DIGIMPLGD
Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The primary aim of the present study is to compare the accuracy of a full digital workflow for dental implants insertion to a partially digital workflow, for a limited edentulous space (1 to 3 dental units), in the maxilla or mandible.

NCT ID: NCT03771248 Not yet recruiting - Clinical trials for Partially Edentulous Mandible

Polyetheretherketone vs Cobalt-chromium Telescopic Removable Partial Denture in Kennedy Class I Patients Regarding Oral Health Related Quality of Life

Start date: January 2019
Phase: N/A
Study type: Interventional

Dentistry is a rapidly progressing field with innumerable advances taking place on a day to day basis. The application of newer technologies and materials has advanced the specialty of prosthodontics and the services rendered to the patients. Taking into consideration that PEEK as a material wasn't clinically investigated to be used as a material for routine use, however PEEK in removable partial dentures will help in making many steps easier and reach patients demands regarding esthetics. Also, owing to the superior mechanical and biological properties of PEEK, it will not be surprising if dentures constructed from the polymer are routinely constructed in near future.

NCT ID: NCT01142297 Completed - Type 2 Diabetes Clinical Trials

Comparative Study of Implant Surfaces to Enhance Stabilization in Patients With Type 2 Diabetes

Start date: July 2008
Phase: N/A
Study type: Interventional

This study compares the patterns of dental implant stabilization between a standard and chemically modified implant surface in patients with type 2 diabetes. It is hypothesized that the chemically modified surface will enhance early healing events (first 4 months following placement)in diabetes patients with compromises in rate of implant integration.