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Immediate Implant With Cusomized Healing Abutment

Evaluation of Immediate Implant Placement Using Customized Healing Abutment (Clinical Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04517968
Enrollment
8
Registered
2020-08-19
Start date
2019-10-01
Completion date
2020-06-15
Last updated
2020-08-19

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

Conditions

Peri-implant Osteogensis

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.

Interventions

OTHERimmediate implant with customized healing abutment

* All patients will be operated under local anesthesia. * Atraumatic extraction of the remaining root or tooth will be achieved. * A careful curettage of the socket will be performed if any granulation tissue is present. * Sequential drilling of the osteotomy site with copious irrigation will be done * The Implant is secured in place using a torque wrench. * Fabrication of the customized abutment with flowable composite by first placing a rubber dam between the abutment and the implant to prevent leakage of composite into the socket then start adding the composite in a manner to seal the socket. * Finishing the composite outside the patient's mouth will be done to ensure the borders are smooth with no sharp ends. * The abutment will be attached to the implant.

Sponsors

Hams Hamed Abdelrahman
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Age range: 20 - 40 years * Good oral hygiene * A freshly extracted socket in the mandibular molar area. * The gap between the implant and the bone will be at least 3-4 mm.

Exclusion criteria

* Acute infection (periodontitis or mucosal infection) * Patients on radiotherapy or chemotherapy. * Alcohol or drug abuse. * Patient with the systemic disorder (uncontrolled Diabetes mellitus, autoimmune diseases, bone diseases, etc.) * Smokers. * Parafunctional habits.

Design outcomes

Primary

MeasureTime frameDescription
change in bone densityat 3rd, 6th monthsCone 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

MeasureTime frameDescription
Change in pain1st day, 1 week, 4 weeks, 6 weeks, 12 weeks and after 6 monthsThe patients will be examined using the Visual Analogue Scale (VAS). the scale is from 0-10 0 =no pain 10= most severe pain

Countries

Egypt

Outcome results

None listed

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