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Alveolar Bone Grafting clinical trials

View clinical trials related to Alveolar Bone Grafting.

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NCT ID: NCT05422196 Completed - Clinical trials for Alveolar Bone Grafting

Evaluation of Computer-Guided Secondary Alveolar Cleft Bone Grafting With and Without Platelet-Rich Fibrin

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

This study aims at investigating the role of platelet-rich fibrin in alveolar cleft secondary grafting. This grafting is done from the patient's chin using a computer-guided stent that is customized for each patient, and the cleft volume is analysed at first to estimate the needed amount of bone to be harvested.

NCT ID: NCT04868825 Active, not recruiting - Clinical trials for Alveolar Bone Grafting

Safety and Efficacy Evaluation of the Ivory Dentin Graft Device (IvoryGraft) - Long Term Follow-Up

Start date: November 7, 2017
Phase: N/A
Study type: Interventional

long-term safety and performance of Ivory Dentin Graft. Ivory Dentin Graft is at least as good as the competitor treatment group (OsteoBiol Gen-Os) for alveolar ridge preservation following tooth extraction.

NCT ID: NCT03549039 Completed - Quality of Life Clinical Trials

Effect of Alveolar Bone Grafting

Start date: June 30, 2018
Phase:
Study type: Observational

This study included patients who underwent secondary alveolar bone grafting by harvesting graft from the anterior iliac crest, in Oral and Maxillofacial Department, Faculty of Dentistry, Ankara University, Turkey, during the period from January 2012 to March 2016. All patients were operated using the same technique and by the same surgical team. Patients will be interviewed to fill Short-Form Health Survey (SF-12) and Postsurgical Patient Satisfaction Questionnaire (PSPSQ) 6 months postoperatively. The questionnaires will be used to assess the relationship between health quality and patient satisfaction. Also, grafted sites will be evaluated with respect to fistula, the presence of cleft palate, and infection.The descriptive statistics and Pearson correlation analyses will be made using PSPSQ scores and SF-12 PCS and MCS scores.

NCT ID: NCT03150472 Completed - Clinical trials for Alveolar Bone Grafting

Safety and Efficacy Evaluation of the Ivory Dentin Graft Device

IvoryGraft
Start date: November 7, 2017
Phase: N/A
Study type: Interventional

Ivory Dentin Graft is at least as good as the competitor treatment group (OsteoBiol Gen Os) for alveolar ridge preservation following tooth extraction. The non-inferiority endpoints will be achieved if the competitor treatment group will not be statistically better than the Ivory Graft treatment.

NCT ID: NCT02526563 Completed - Clinical trials for Alveolar Bone Grafting

Serum Ropivacaine Concentrations in Pediatric Patients Receiving Continuous Wound Catheter Analgesia

Start date: August 2015
Phase:
Study type: Observational

The primary investigators in this study plan to investigate serum concentrations of ropivacaine in pediatric patients who already receive as standard of care a continuous wound catheter after an iliac crest alveolar bone graft harvest for completion of a previous cleft palate repair. The goals of this study are 1) to determine serum concentrations (free, unbound) of ropivacaine 2) To evaluate pain scores during the perioperative period to determine efficacy of wound catheters for postoperative analgesia for iliac crest bone graft harvest.

NCT ID: NCT02444052 Completed - Dental Implant Clinical Trials

Evaluation of Zimmer Puros® Allograft vs. Creos™ Allograft for Alveolar Ridge Preservation

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

The purpose of this study is to evaluate clinically, histologically and radiographically the healing of extraction sockets with Zimmer's Puros® allograft compared to creos™ (creo™ Nobel Biocare,), a low-cost allograft material, 90 days following exodontia.

NCT ID: NCT02406924 Not yet recruiting - Bone Augmentation Clinical Trials

Bone Augmentation Using Particulated Biomaterial and Autogenous Bone, Stabilized by Collagen Membrane and Pins (PaMP)

PaMP
Start date: April 2015
Phase: N/A
Study type: Interventional

Twenty four patients with bone resorption on the anterior maxilla will be divided into two groups with different kinds of grafting: bone block associated with particulated biomaterial and particulated mixture of autogenous bone and biomaterial stabilized by collagen membrane and pins. The techniques will be compared according to volume gain, quality of graft osseointegration, implant survival and maintenance of the level of soft tissues.