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Bone Resorption clinical trials

View clinical trials related to Bone Resorption.

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NCT ID: NCT03052387 Not yet recruiting - Bone Resorption Clinical Trials

Vertical Augmentation Using Onlay Versus Inlay Autogenous Graft With Simultaneous Implant Placement.

Start date: March 2017
Phase: N/A
Study type: Interventional

Using autogenous Chin block for vertical augmentation with simultaneous implant placement at anterior maxilla region comparing between the Onlay and Inlay grafting techniques.

NCT ID: NCT03049137 Not yet recruiting - Bone Resorption Clinical Trials

Computer Guided Versus Conventional Augmentation Using Bone Ring

Start date: February 2017
Phase: N/A
Study type: Interventional

Using bone ring grafts with simultaneous implant placement after three-dimensional augmentation of severely defective bone ridges using computer-guided surgical templates. The study compares accuracy effectiveness by mimics software

NCT ID: NCT03028038 Completed - Bone Resorption Clinical Trials

Using Platelet Rich Plasma in Reducing Alveolar Bone Resorption During Rapid Maxillary Expansion

Start date: July 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if the injection of Platelet-rich plasma (PRP) is effective in reducing alveolar bone loss that happens after each rapid maxillary expansion (RME) on the buccal aspect of the posterior teeth. 16 patients with a skeletal maxillary constriction aged between 10-16 years old will get into orthodontic treatment to widen the maxilla using Hyrax appliance. An amount of patient blood will be withdrawn and centrifuged to get PRP. Then the PRP will be injected in one half of each patient mouth in a split-mouth design, beneath the buccal periosteal of the first molars and first premolars, the halves will be chosen randomly. High resolution CBCT images will be taken before and after orthodontic treatment to analyze buccal bone thickness and height changes.

NCT ID: NCT03026894 Completed - Bone Resorption Clinical Trials

Association of Force Distribution and Bone Resorption

Start date: November 2015
Phase: N/A
Study type: Interventional

To investigate the residual ridge resorption at anterior and posterior maxillary and posterior mandibular ridges among conventional complete dentures and implant overdenture wearers, and determine its association with the relative occlusal forces distribution, treatment groups and other patient variables.

NCT ID: NCT03014388 Not yet recruiting - Bone Resorption Clinical Trials

Posterior Maxillary Ridge Augmentation With Sinus Lift Using Mineralized Plasmatic Matrix Versus Autogenous Bone Graft

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

Using growth factors obtained from patient's venous blood mixed with particulate autogenous bone the study compares bone gain by implant with gold standards in sinus Lift procedures for future implant insertion.

NCT ID: NCT03007069 Not yet recruiting - Bone Resorption Clinical Trials

Preimplant Site Augmentation Using MPM Versus Autogenous Bone Graft

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

Using growth factors obtained from patient's venous blood mixed with particulate autogenous bone the study compares bone gain by implant with gold standards.

NCT ID: NCT02982681 Completed - Clinical trials for Periodontal Diseases

Bioactive Glass and Platelet Rich Fibrin in Intrabony Defects

Start date: April 2015
Phase: Phase 3
Study type: Interventional

Background: Platelet-rich fibrin (PRF) and bioactive glass putty has been shown to be effective in promoting reduction in probing depth, gain in clinical attachment, and defect fill in intrabony periodontal defects. The individual role played by bioactive glass putty in combination with PRF is yet to be elucidated. AIM: To compare the clinical effectiveness of the combination of Plaltelet Rich Fibrin and Bioactive Glass Putty and Bioactive glass putty regenerative techniques for intrabony defects in humans. Material and methods: Ten pairs of intrabony defects were surgically treated with PRF and Bioactive glass putty (Test group) on one side or bioactive glass putty (Control group) on other side. The primary outcomes of the study included changes in probing depth, attachment level and bone fill of Osseous defect. The clinical parameters were recorded at baseline, 3, 6, and 9 months. Radiographic assessment was done using standardized intra oral periapical radiographs. Comparisions were made within each group between baseline, 3 months, 6 months and 9 months using the ANOVA test followed by Bonferroni test.

NCT ID: NCT02937220 Not yet recruiting - Clinical trials for Single Tooth Dental Implant

Influence of Superstructure Material on Crestal Bone Resorption and Esthetic Outcome of Dental Implants

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

The aim of this study is to evaluate the influence of superstructure material on crestal bone resorption and esthetic outcome of dental implants in patients with single missing tooth in the aesthetic zone.

NCT ID: NCT02903667 Recruiting - Bone Resorption Clinical Trials

Biomaterial to Counteract Ridge Reduction Following the Removal of Multiple Adjacent Teeth.

Biomaterial
Start date: March 2015
Phase: N/A
Study type: Interventional

An open, prospective, randomized, multicenter study focused on the ridge diminution in case of grafting of fresh extraction sockets with Bio-Oss Collagen, Bio-Gide (Geistlich Pharma, Wolhusen, Switzerland), placing Dentsply implants (Astra Tech System).

NCT ID: NCT02867982 Active, not recruiting - Bone Resorption Clinical Trials

Platform Switched Implant and Bone Level Alteration

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

This is a two-year prospective randomized clinical study to to evaluate whether the gingival thickness and insertion depth of dental implants have any influence on marginal bone levels changes around platform switched implants.