Actively Recruiting
All-on-X Full-arch Implant-supported Rehabilitation Using Stackable Surgical Guides for Maxillary Terminal Dentition Retrospective 2-year Analysis
Led by Menoufia University · Updated on 2026-01-20
40
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
M
Menoufia University
Lead Sponsor
M
Mansoura University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the clinical performance of maxillary All-on-X full-arch implant-supported rehabilitation using a fully digital stackable guided surgery and immediate loading protocol. This retrospective study focuses on patients with terminal maxillary dentition treated with this approach, aiming to assess implant survival and peri-implant outcomes over a two-year follow-up. The study also investigates how surgical and prosthetic factors, including basal seating guide design, influence these results. Patients received a maxillary All-on-6 implant-supported complete fixed dental prosthesis planned through three-dimensional imaging and dedicated software. Stackable surgical guides were used to enable guided bone reduction when needed, followed by fully guided implant placement under local anesthesia. Implants with sufficient primary stability were immediately loaded with a screw-retained provisional fixed prosthesis on multi-unit abutments. The treatment followed a standardized surgical protocol with occlusal contacts minimized during healing. Participants are followed for at least two years with scheduled clinical and radiographic assessments at prosthesis delivery, one year, and two years. Outcome measures include implant survival at six months post-placement, peri-implant clinical parameters such as plaque index, bleeding on probing, probing depth, and marginal bone level changes assessed by standardized radiographs. The study collects complete clinical and radiographic records to evaluate success according to established criteria.
CONDITIONS
Brief Title
All-on-X Stackable Guides for Maxillary Terminal Dentition
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients presenting with terminal dentition of the maxillary arch
- Rehabilitation with a maxillary All-on-6 implant-supported complete fixed dental prosthesis
- Treatment performed using a fully digital stackable guided surgery workflow
- Immediate loading with a provisional fixed prosthesis
- Availability of complete clinical and radiographic records
- Minimum follow-up period of 2 years
- Prosthetic design classified as FP-1 or FP-2 according to Misch classification
You will not qualify if you...
- Uncontrolled systemic conditions contraindicating implant surgery
- History of head and neck radiotherapy
- Presence of untreated periodontal or peri-implant infection at the time of surgery
- Incomplete or missing clinical or radiographic records
- Cases requiring simultaneous bone grafting procedures
- Severe maxillary atrophy (Cawood and Howell Class III-V)
- Cases requiring FP-3 prosthetic design
- Rehabilitation performed without guided surgery or without immediate loading
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 - 1 day
Participants undergo maxillary full-arch implant rehabilitation using a fully digital stackable guided surgery workflow with immediate loading of a provisional fixed prosthesis.
1 surgical visit (in-person)
Duration - 2 years
Participants are followed according to a predefined clinical and radiographic protocol to monitor implant success and peri-implant health.
Visits at prosthesis delivery, 6 months, 1 year, and 2 years post-implant placement
Trial Site Locations
Total: 1 location
1
Faculty of Dentistry
Shibīn al Kawm, Menoufia, Egypt
Actively Recruiting
Research Team
M
Mohammed El-Sawy, PhD
M
Mohammed T. Khater, 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
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here