Skip to main content
Clinical Trials/NCT05066815
NCT05066815UnknownNot Applicable

Evaluation of Crestal Bone Loss Around Short Dental Implants As Affected By Two Suprastructure Materials

Cairo University0 sites20 target enrollmentStarted: October 25, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
20
Primary Endpoint
Crestal Bone Loss Crestal bone loss will be measured using standardized digital periapical radiograph by paralleling technique and film holding device -measuring unit:Milimeters

Study Overview

Brief Summary

The aim of the study is to evaluate the crestal bone loss developed around short dental implants after using screw retained Hybrid ceramic crowns when compare to screw retained Lithium Di silicate based ceramic crowns.

Detailed Description

This study will be conducted on patients requiring single implant replacement in the posterior regions of the mandible, admitted to the Outpatient Clinic of Fixed Prosthodontics Department, Faculty of Oral and Dental medicine, Cairo University.

Examination and diagnosis:

  1. Selection and examination of the patients according to inclusion and exclusion criteria.
  2. Preoperative Cone Beam Computed Tomography (CBCT) to all patients.
  3. Primary impression will be taken to produce study cast.
  4. Taking a professional photo for the examined posterior area.
  5. Patients will be divided into two group:

G1: Short implants will be restored by screw retained Hybrid ceramic crowns G2: Short implants will be restored by screw retained Lithium Di silicate based ceramic crowns

Surgical procedures:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Patients within age group of ≥
  • There should be absence of any systemic diseases.
  • Patients have missing simple posterior tooth
  • Adequate interarch space.
  • Inadequate residual bone height to place standard length implant.
  • Patients with good oral hygiene.

Exclusion Criteria

  • A history that would complicate the outcome of the study, such as alcohol or drug dependency, smoking, poor health, or any other medical, physical or psychological reason that might affect the surgical procedure or the subsequent prosthodontics treatment and required follow-up.
  • Heavy smokers.
  • Poorly controlled diabetes mellitus.
  • Patients on radiotherapy.
  • Patients with temporomandibular disorders

Arms & Interventions

Hybrid superstructure

Experimental

screw retained hybrid ceramic crowns

Intervention: Vita Enamic (Hybrid dental ceramic) (Other)

Ceramic superstructure

Active Comparator

screw retained lithium disilicate based ceramic crowns

Intervention: Vita Enamic (Hybrid dental ceramic) (Other)

Outcomes

Primary Outcomes

Crestal Bone Loss Crestal bone loss will be measured using standardized digital periapical radiograph by paralleling technique and film holding device -measuring unit:Milimeters

Time Frame: one year

preventive

Secondary Outcomes

  • screw loosening of crowns screw loosening will be observed by clinical investigation -measuring unit:Binary (Yes/No)(one year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dina Nabil Ezz Eldin

: Assistant Lecturer of Fixed Prosthodontics, Faculty of Dentistry (Aswan University)

Cairo University

Similar Trials