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Edentulous Alveolar Ridge clinical trials

View clinical trials related to Edentulous Alveolar Ridge.

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NCT ID: NCT06034067 Active, not recruiting - Clinical trials for Dental Implant Failed

Osseodensification Versus Conventional Drilling for Implant Site Preparation

Start date: September 1, 2022
Phase: N/A
Study type: Interventional

A total of 34 participants, who require replacement of an anterior or posterior single tooth with dental implant, will be randomly allocated to two equal sized groups. In the control group, the osteotomy site preparation will be prepared by using conventional surgical drills, while the test group site preparation will involve the use of Densah™ Burs (Versah Co., LLC., USA) as per the osseodensification protocol. In addition to evaluating implant stability, the trial will also report on implant and patient outcomes at various time points.

NCT ID: NCT05960916 Active, not recruiting - Clinical trials for Edentulous Alveolar Ridge

Primary Stability of Immediate Implant Using Versah Versus Conventional Burs

Start date: January 22, 2022
Phase: N/A
Study type: Interventional

This study is designed as a Prospective Randomized Clinical Trail, Evaluate the effect of osseodensification technique on primary stability in comparison to the conventional drilling technique in immediate single fresh extraction sockets.

NCT ID: NCT05219305 Active, not recruiting - Clinical trials for Edentulous Alveolar Ridge

Implant Stability in Autogenous Mineralized and Demineralized Dentin Grafts

Start date: April 1, 2022
Phase: N/A
Study type: Interventional

The bone grafting materials currently used in dentistry are autografts, allografts, xenografts, and alloplastic grafts. Among these different types of bone graft materials, autografts are considered to have the most predictable results due to their properties of osteogenesis, osteoinduction, and osteoconduction. However, bone autografts are rarely used due to the high morbidity associated with harvesting the bone graft from the patient with a second surgical site. Because of the increased risk to the patient with autogenous bone grafts, the current standard of care is an allograft, which is a bone graft harvested from cadaver sources such as Freeze-Dried Bone Allograft (FDBA). While allografts can only possess the qualities of osteoinduction and osteoconduction, they also have dramatically less morbidity due to the lack of a second surgical site. Our null hypothesis states that: Experimental groups (mineralized, and partially demineralized dentin grafts) do not show positive changes in implant stability, survival, failure rate, probing pocket depth, and interproximal crestal bone level changes when compared to FDBA Our alternative hypothesis states that: Experimental groups (mineralized, and partially demineralized dentin grafts) show similar or better results in terms of implant stability, survival, failure rate, probing pocket depth, and interproximal crestal bone level changes when compared to FDBA.

NCT ID: NCT04006782 Active, not recruiting - Clinical trials for Edentulous Alveolar Ridge

Narrow Dental Implants in Multiple Fixed Prosthesis: A Controlled Clinical Trial

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

The objective of this study is to evaluate the survival of narrow dental implants (≤ 3,5 mm) in multiple fixed prostheses in comparison with standard diameter dental implants (≥ 3,75 mm) after 5 years of follow-up. The hypothesis of the study is that narrow dental implants under the evaluated conditions, have the same survival rate and clinical performance than the standard diameter implants.

NCT ID: NCT03177356 Active, not recruiting - Clinical trials for Edentulous Alveolar Ridge

Implant Placement in Mandibular Molar Xenograft Versus PRF

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

20 recruited patients indicated for immediate implant placement in mandibular molar patients are divided into 2 groups each group contain 15 patients, one group assigned for placement of bovine bone after molar extraction and immediate implant placement, while the other group we use Platelet-rich fibrin as space filling material.