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Horizontal Ridge Deficiency clinical trials

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NCT ID: NCT06195761 Not yet recruiting - Clinical trials for Horizontal Ridge Deficiency

Computer Guided Modified Ridge Splitting Versus Free Hand Technique in Horizontal Deficiency in Posterior Mandible

Start date: May 15, 2024
Phase: N/A
Study type: Interventional

To assess the accuracy of the computer assessed guides in horizontal bone augmentation achieved at posterior mandible using guided modified ridge splitting technique versus free hand modified ridge splitting technique

NCT ID: NCT06186232 Not yet recruiting - Clinical trials for Horizontal Ridge Deficiency

Evaluation of Bone Regenerated With Guided Bone Regeneration (GBR) Using Polymethylmethacrylate (PMMA) Membrane

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

To evaluate the quantity and quality of bone generated, radiographically and histomorphometrically, after guided bone regeneration (GBR) using a membrane of 3D printed custom made (PMMA) and subsequent stability of delayed implant placement.

NCT ID: NCT06043258 Completed - Clinical trials for Horizontal Ridge Deficiency

Bond Apatite in Horizontal Augmentation Versus Bio-Oss

BondApatite
Start date: October 10, 2020
Phase: N/A
Study type: Interventional

Sixteen healthy patients selected from the Outpatient Clinic of the Department of Oral Medicine, Periodontology, Diagnosis and Oral Radiology, Faculty of Dentistry, Mansoura University for the replacement of missing single maxillary anterior or premolar tooth (in the esthetic zone) by dental implant. Patients were selected according to the following criteria: 1) Patients older than 18 years. 2) Good general health, with no systemic diseases that might contraindicate receiving a dental implant. 3) Every patient should have at least one missing tooth in the maxillary anterior premolar area and subsequently scheduled for implant supported prosthesis. 4) The tooth has been extracted from at least 3 months. 5) Insufficient horizontal bone (class III according to Len Tolstunov classification. 6) Good oral hygiene. Patients were classified into two groups: Group (I) (study group): eight patients with missing anterior or premolar tooth with insufficient horizontal (bucco/labio palatal) bone width were treated with dental implants and Bond Apatite (AugmaBio, United States of America) as a bone graft material to fill the defect. Group (II) (positive control group): eight patients with missing anterior or premolar tooth with insufficient horizontal (bucco/labio palatal) bone width were treated with dental implants and Bio-Oss (Bio-Oss, GeistlichPharmaAG, Wolhusen, Switzerland) as a bone graft material to fill the defect and pericardium resorbable membrane. Patients were evaluated with the following clinical and radiological parameters presurgical and 12 months after operation: A) Clinical evaluation: The following parameters were evaluated: 1. Modified plaque index: This is fundamentally based on the visual detection of plaque, it ascertains the thickness of plaque along the gingival margin, namely the desirability of distinguishing clearly between severity and the location of soft debris aggregates. 2. Modified gingival index: It is a method to assess the severity of gingivitis based on gingival color, contour, presence of bleeding, stippling and crevicular fluid flow. It is completely noninvasive method (only visual). 3. Probing depth: Peri-implant pocket depth was measured using plastic implant probe (contrast PA probe # CPNG22, Helmut Zepf Medizintechnik Gmbh®) after final restoration was inserted. B) Radiographic evaluation: Bone width was assessed using CBCT 12 months after implant insertion. Bone width measurements were made on tomographic slices perpendicular to the longitudinal axis of the alveolar crest; 2 mm from the alveolar crest.

NCT ID: NCT05813340 Recruiting - Clinical trials for Horizontal Ridge Deficiency

Vascularized Inter-positional Periosteal Connective-tissue Flap Versus Collagen Membrane in Guided Bone Regeneration

VIP-CT
Start date: January 1, 2023
Phase: N/A
Study type: Interventional

this study compares 2 techniques in guided bone regeneration for horizontal ridge augmentation in aesthetic zone

NCT ID: NCT05418452 Recruiting - Clinical trials for Horizontal Ridge Deficiency

Efficacy of 1% Metformin Gel Mixed With PRF in Augmenting Narrow Ridge

MF
Start date: June 15, 2022
Phase: Phase 3
Study type: Interventional

This study aimed to evaluate the efficacy of 1% metformin gel mixed with PRF, in horizontal ridge augmentation with the split-crest technique, for implant placement.

NCT ID: NCT05311332 Completed - Clinical trials for Alveolar Bone Resorption

Computer-guided vs. Conventional Cortical Shell Technique for Horizontal Augmentation

Start date: October 13, 2021
Phase: N/A
Study type: Interventional

this study aims to evaluate horizontal bone augmentation achieved at the anterior maxilla using computer-guided cortical shell bone technique and accuracy of fixation of the bone shell away from the atrophic ridge by a calculated distance which is always a challenging step for inexperienced surgeons to fix a cortical shell at the ideal position in the conventional protocol it was never guided to be precisely fixed at the proper position and angulation the problem is if it fixed with insufficient distance with proposed volume loss leads to totally insufficient volume gain for future implant placement also to evaluate the efficacy of the CAD/CAM surgical guide during chin harvesting procedures in reducing the risk of anatomical structure damage and patient morbidity with more accuracy compared with the standard technique. this trial versus free hand conventional cortical shell bone technique both harvested from symphysis area (chin).

NCT ID: NCT05286541 Completed - Clinical trials for Horizontal Ridge Deficiency

Buccal Cortical Separation and Lateralization for Horizontal Ridge Augmentation

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

Cases with horizontal ridge deficiency less than what is possible for ridge splitting were recruited and the buccal cortex was totally separated and lateralized at the desired distance for augmentation

NCT ID: NCT05013580 Completed - Clinical trials for Horizontal Ridge Deficiency

The "Open Wound Bone Augmentation Concept" With Amnion-Chorion Membrane

Start date: October 8, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two bone graft wound healing techniques; an open wound healing approach versus the standard closed wound healing approach.

NCT ID: NCT04748952 Completed - Clinical trials for Horizontal Ridge Deficiency

Ridge Expansion by Osseodensification

Start date: January 26, 2021
Phase:
Study type: Observational

A prospective observational clinical study guided by the guidelines of Strengthening the Reporting of Observational Studies in Epidemiology (STORBE) in 2014, that conducted to assess amount of ridge expansion obtained by using Dansah burs with simultaneous implant placement.

NCT ID: NCT04376060 Completed - Clinical trials for Horizontal Ridge Deficiency

The Horizontal Ridge Augmentation Using Equine Xenograft and a Collagenated Porcine Cortical Lamina

Start date: April 4, 2017
Phase: N/A
Study type: Interventional

The primary aim of this study is to clinically, radiographically and histologically evaluate the lateral bone augmentation of the soft porcine cortical lamina (OsteoBiol®) using equine-derived bone particles (OsteoBiol®)