Actively Recruiting
Accuracy of Standard and Geometric Pattern-Assisted Digital Scanning for Full-Arch Implant Prosthesis Frameworks
Led by Mirna ashraf anis heneen · Updated on 2025-07-15
4
Participants Needed
1
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This clinical trial aims to compare three different impression techniques used to fabricate full-arch implant-supported dental prostheses. Accurate impressions are essential to ensure a passive and precise fit of the final prosthetic framework, which contributes to long-term implant success and patient comfort. In this crossover study, participants with four osseointegrated dental implants in the lower jaw will undergo three types of impressions: Conventional splinted impression using polyvinyl siloxane (PVS) material. Standard digital impression using an intraoral scanner. Geometric pattern-assisted digital impression, which incorporates a visual reference pattern to improve scan alignment and accuracy. Each participant will receive all three impression techniques in a randomized sequence, at different time points. The accuracy of each method will be assessed by evaluating the passivity of the resulting prosthetic frameworks using two methods: (1) digital superimposition analysis to measure three-dimensional (3D) spatial deviation, and (2) the clinical "one-screw test" to detect misfit. The study seeks to determine whether digital scanning, particularly with geometric pattern assistance, can provide accuracy comparable to or better than conventional methods. Findings may guide improvements in digital prosthodontic workflows and support more efficient, predictable treatment outcomes.
CONDITIONS
Official Title
Accuracy of Standard and Geometric Pattern-Assisted Digital Scanning for Full-Arch Implant Prosthesis Frameworks
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 30 to 70 years
- Completely edentulous mandible
- Presence of four osseointegrated implants in the lower jaw
- Good oral and general health
- Willingness to participate and provide written informed consent
- Availability for all study appointments
You will not qualify if you...
- Systemic diseases or conditions that affect bone healing or implant integration
- Presence of oral inflammation, infection, or soft tissue abnormalities at implant sites
- History of bruxism or parafunctional habits
- Inability to understand or comply with study procedures
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Mansoura University
Al Mansurah, Dakahlia Governorate, Egypt, 35516
Actively Recruiting
Research Team
M
Mirna A. Anis
CONTACT
K
Khaled M. Zahran
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
DIAGNOSTIC
Number of Arms
3
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