Actively Recruiting

Age: 60Years - 80Years
All Genders
ID07534514

Digitally Assisted Immediate Implant Placement and Loading in Geriatric Patients

Led by Menoufia University · Updated on 2026-04-16

40

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the clinical performance of digitally assisted immediate implant placement and immediate loading in elderly patients aged 65 years and older who require tooth extraction. This study aims to assess biological outcomes such as implant survival and changes in marginal bone levels, alongside mechanical complications and the progression of primary implant stability. Patient-reported outcomes including pain, functional improvement, and esthetic satisfaction are also being measured using visual analog scales. The goal is to determine how well this treatment approach works in the geriatric population. The treatment involves a fully digital workflow that uses cone beam computed tomography (CBCT), intraoral scanning, and computer-aided design/computer-aided manufacturing (CAD/CAM) generated tooth-supported surgical guides to assist in precise implant placement. Surgical procedures use minimally invasive techniques, and immediate provisional restorations are placed within 48 hours, with adjustments made to control loading based on implant stability. Definitive prostheses are delivered after 3 to 6 months, and minor peri-implant gaps may be grafted as needed. Participants will be followed for 12 months with regular clinical and radiographic evaluations. Assessments include implant survival rate and marginal bone level changes at baseline, 6 months, and 12 months. Secondary outcomes include biological complications like peri-implant mucositis, mechanical issues such as screw loosening, and patient satisfaction measures. The study collects data on insertion torque and implant stability quotient (ISQ) to monitor primary stability, aiming to provide evidence on the safety and predictability of this digital approach in elderly patients.

CONDITIONS

Brief Title

Digitally Assisted Immediate Implants in Geriatric Patients

Who Can Participate

Age: 60Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 65 years and older
  • Need for tooth extraction with immediate implant placement
  • Sufficient residual bone volume to achieve implant stability
  • Ability to achieve insertion torque of at least 35 Ncm and/or implant stability quotient (ISQ) of 60 or higher
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Adequate oral hygiene and patient compliance
Not Eligible

You will not qualify if you...

  • Uncontrolled systemic diseases such as uncontrolled diabetes mellitus
  • History of head and neck radiotherapy
  • Active untreated periodontal disease
  • Heavy smoking (more than 10 cigarettes per day)
  • Current or previous bisphosphonate therapy
  • Parafunctional habits such as severe bruxism

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 48 hours

Participants undergo digitally assisted immediate implant placement using a fully digital workflow including CBCT, intraoral scanning, and CAD/CAM surgical guides. Immediate provisional restorations are delivered within 48 hours with occlusal adjustments to control loading.

1 surgical visit and 1 visit within 48 hours for provisional restoration

Post-operative Follow-up

Duration - 12 months

Participants are followed clinically and radiographically to assess implant survival, bone level changes, and complications. Definitive prostheses are delivered after 3 to 6 months.

Scheduled visits at baseline, 6 months, and 12 months post-implantation

Trial Site Locations

Total: 1 location

1

Mohammed Elsawy

Shibīn al Kawm, Menoufia, Egypt, 2266166

Actively Recruiting

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Research Team

M

Mohammed A. Elsawy, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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