Immediate Implant With Cusomized Healing Abutment

Not Applicable

Completed

• Conditions: Peri-implant Osteogensis
• Interventions: Other: immediate implant with customized healing abutment

• Registration Number: NCT04517968
• Lead Sponsor: Hams Hamed Abdelrahman

Brief Summary

evaluate clinically and radiographically the effect of customized healing abutment on peri-implant osteogenesis following immediate implant placement.

Detailed Description

Now a day most people want to make immediate implant after extraction, which save them time and eliminates the need of second surgery. The problem is that the jummping gap between the implant and the bone that needs bone graft, this increase the cost on the patient. In this experiment we tend to evaluate this technique which may help us in growing autogenous bone and stop the need for bone grafting.

The aim of this study is to evaluate clinically and radiographically the effect of customized healing abutment on peri-implant osteogenesis following immediate implant placement.

A clinical trial was carried out on 8 patients (20-40 years old) with freshly extracted mandibular molars. Implants were placed immediately after extraction and a customized healing abutment will be fabricated. Patients were followed up clinically and radio graphically for 6 months.

Study Timeline

• Study Start: 2019-10-01
• Primary Completion: 2020-02-03
• Study Completion: 2020-06-15
• Status Verified: 2020-08
• Study First Submitted: 2020-08-14
• Study First Submitted QC: 2020-08-17
• Last Update Submitted: 2020-08-17
• Study First Posted: 2020-08-19
• Last Update Posted: 2020-08-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 8

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
immediate implant with customized healing abutment	immediate implant with customized healing abutment	-

Primary Outcome Measures

Name	Time	Method
change in bone density	at 3rd, 6th months	Cone beam CT will be taken immediately and 6 months postoperatively On Demand 3d software\*\* is used to assess: 1. Crestal bone loss.; 2. Perapical Bone density.

Secondary Outcome Measures

Name	Time	Method
Change in pain	1st day, 1 week, 4 weeks, 6 weeks, 12 weeks and after 6 months	The patients will be examined using the Visual Analogue Scale (VAS). the scale is from 0-10 0 =no pain 10= most severe pain

Trial Locations

Locations (1)

Faculty of Dentistry; 🇪🇬 Alexandria, Egypt