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Clinical Trials/NCT05974215
NCT05974215
Completed
N/A

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

Menatallah Mohamed Elhotieby1 site in 1 country10 target enrollmentApril 1, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Implant Site Reaction
Sponsor
Menatallah Mohamed Elhotieby
Enrollment
10
Locations
1
Primary Endpoint
assessment of change of bone height around dental implants
Status
Completed
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 1, 2023
End Date
July 5, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Menatallah Mohamed Elhotieby
Responsible Party
Sponsor Investigator
Principal Investigator

Menatallah Mohamed Elhotieby

researcher fixed and removable prosthodontics

National Research Centre, Egypt

Eligibility Criteria

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.

Outcomes

Primary Outcomes

assessment of change of bone height around dental implants

Time Frame: on the first day, on 30th day, 90th day

bone height was assessed by cone beam computed tomography

assessment of change of bone density around dental implants

Time Frame: on the first day, on 30th day, 90th day

bone density was assessed by cone beam computed tomography

Study Sites (1)

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