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

Bone Loss Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05066815
• Other study ID #: 211020
• Status: Not yet recruiting
• Phase: N/A
• Start date: October 25, 2022
• Est. completion date: December 1, 2023

Study information

• Verified date: June 2022
• Source: Cairo University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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:

• Implants will be placed following standardized protocol.

• After 4 months the patients re-attended for placement of healing abutments for about (10-14) days and prosthesis fabrication.

Data collection and post operative radio-logical assessment:

-Taking standardized digital peri-apical radio-graph by paralleling technique and film holding device for follow up at 12 months after crowns loading to evaluate crestal bone loss.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: December 1, 2023
• Est. primary completion date: December 25, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients within age group of = 18.

2. There should be absence of any systemic diseases.

3. Patients have missing simple posterior tooth

4. Adequate interarch space.

5. Inadequate residual bone height to place standard length implant.

6. Patients with good oral hygiene.

Exclusion Criteria:

1. 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.

2. Heavy smokers.

3. Poorly controlled diabetes mellitus.

4. Patients on radiotherapy.

5. Patients with temporomandibular disorders

Related Conditions & MeSH terms

• Bone Diseases, Metabolic
• Bone Loss

Intervention

Other:
• Vita Enamic (Hybrid dental ceramic)
Vita Enamic (Hybrid dental ceramic) is provided as blocks to be milled using Computer aided design/Computer aided manufacturer (CAD/CAM) technology.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Crestal Bone Loss Crestal bone loss will be measured using standardized digital periapical radiograph by paralleling technique and film holding device -measuring unit:Milimeters	preventive	one year
Secondary	screw loosening of crowns screw loosening will be observed by clinical investigation -measuring unit:Binary (Yes/No)	preventive	one year