Bone Density & Marginal Bone Height Changes Around Dental Implants

Status Completed

Clinical Trial Summary

The increased benefits to the edentulous population from implant supported overdenture is overwhelming in terms of better quality of life, emotional stability, improved function, enhanced esthetics and clinical comfort.1-6 Implant supported prosthesis is considered a viable option for partially edentulous patients7. The oral rehabilitation of a long anterior mandibular edentulous span with a fixed or removable implant-supported prosthesis using appropriate prostheses have been a target in oral implant research for the last year. The longevity of any implant prosthesis depends on successful osseointegration and implant stability. Cone beam computed tomography (CBCT ) has also been used extensively for the follow-up of dental implants and is considered one of the tools for assessing implant success

Clinical Trial Description

This study will be conducted on 6 patients having mandibula Kennedy Class VI (anterior edentulous span) Each patient will receive 5 dental implants in the interforaminal area. The patients will be randomly categorized into two groups. According to the final restoration they will receive. Group I: will receive a digital milled implant supported overdenture. While Group II will receive implant supported fixed bridge. The marginal bone height changes and bone density around the dental implants will be evaluated at the time of prosthesis insertion, after one and three month. Research Procedures: 1. Patient selection: will be following inclusion and exclusion criteria. 2. 5 implants will be installed in the interforaminal area for each patient. 3. Digital impression, bite registration, try in and delivery of the final prosthesis for each group will follow the conventional methods. 4. The marginal bone height changes and bone density around the dental implants using CBCT will be evaluated at the time of prosthesis insertion, after one and three month. 5. Statistical analysis: Data will be collected, tabulated, and statistically analyzed using Microsoft Excel ® 2016, Statistical Package for Social Science (SPSS)® Ver. 24. and Minitab ® statistical software Ver. 16. ;

Study Design

Related Conditions & MeSH terms

Implant Site Reaction

Clinical Trial Details

NCT number	NCT06151314
Study type	Interventional
Source	National Research Centre, Egypt
Contact
Status	Completed
Phase	N/A
Start date	December 1, 2022
Completion date	December 5, 2023

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See also
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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Bone Density and Marginal Bone Height Changes Around Dental Implants

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms