Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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