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Peri Implant Marginal Bone Height and Bone Density

Peri Implant Marginal Bone Height and Density Supporting Different Prosthesis Restoring Single Edentulous Mandible

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05974215
Enrollment
10
Registered
2023-08-03
Start date
2023-04-01
Completion date
2023-07-05
Last updated
2023-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Implant Site Reaction

Keywords

Bone height, Bone density, Implant supported

Brief summary

This study aims to evaluate the effect of mandibular implant supported removable overdenture on bone height and density and compare it with implant supported fixed overdenture in single mandibular overdenture.

Detailed description

In this study 10 patients will be selected following inclusion and exclusion criteria. In each group 5 patients (each patient will receive 6 implants) will be divided randomly into two groups. Group I patients will receive mandibular implant supported removable overdenture, while Group II will receive mandibular implant supported fixed overdenture. All patients will be given the usual home care instructions about wearing and caring of dentures and opposing arch. Regarding dentures, removal of them at night and cleaning with denture brush and mild soap will be required. Measurements of Bone height and Bone density will be obtained by using Cone Beam Computed Tomography (CBCT). Measurements will be obtained at denture insertion, after 1 month and after 3 months.

Interventions

DEVICEassessment of change in bone height by cone beam computed tomography

bone height was measured at 1 ,30 ,90 days after denture insertion

Sponsors

Menatallah Mohamed Elhotieby
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

each patient was not informed about type of received restoration

Intervention model description

group 1 mandibular implant supported overdenture group 2 mandibular implant supported fixed overdenture

Eligibility

Sex/Gender
MALE
Age
40 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Non-smoker Patients * Highly cooperative and motivated patients. * Patients Systemically free from any immunosuppressive diseases.

Exclusion criteria

* Diabetic, hypertensive, cancer patients. * Mandibular arch with thin knife edge, flat or flabby ridge, recent extractions and foreign bodies. * Patients with temporo-mandibular joint disorders and bad oral habits.

Design outcomes

Primary

MeasureTime frameDescription
assessment of change of bone height around dental implantson the first day, on 30th day, 90th daybone height was assessed by cone beam computed tomography
assessment of change of bone density around dental implantson the first day, on 30th day, 90th daybone density was assessed by cone beam computed tomography

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026