Actively Recruiting
The Use of a New Stereophotogrammetry System to Capture Intra-operative Complete-arch Impression for Prosthetic Complications
Led by University of Rome Tor Vergata · Updated on 2025-03-07
10
Participants Needed
1
Research Sites
9 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate a new stereophotogrammetry system designed to capture precise impressions during complete arch dental restorations. Patients who require full arch restorations will be treated using this advanced digital technology, which records implant positions for the delivery of a fixed screw-retained interim prosthesis. The study is observational and focuses on prosthetic complications and prosthesis failure in dental patients. The study uses a device called FAST MAP that applies a full digital workflow with stereophotogrammetry intraoral impression to immediately load complete arch restorations. Patients receive their treatments using this system, which captures accurate implant positions to produce the interim prosthesis. This approach aims to streamline the restoration process by integrating dynamic navigation and digital impression techniques. Participants will be monitored for prosthetic success over a period of three months following the procedure. Researchers will assess outcomes related to the precision of implant positioning and the success of the prosthetic restoration. The study is open to healthy adults and includes evaluations of oral health indices and bone measurements to ensure suitability. Follow-up includes regular assessments to track the stability and function of the dental prosthesis.
CONDITIONS
Brief Title
New Stereophotogrammetry System to Capture Complete-arch Impression
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Healthy patients aged 18 years or older
- Full mouth bleeding and plaque index of 25% or less
- Bone height suitable for implants at least 10 mm long
- Bone width of at least 5 mm for narrow implants and 6 mm for regular implants
- Fresh extraction sockets with intact buccal wall
- At least 4 mm and 5 mm of bone beyond the root apex in the mandible and maxilla respectively
- Minimum insertion torque of 45 Ncm
You will not qualify if you...
- General medical or psychiatric contraindications (ASA class III or IV)
- Pregnancy or breastfeeding
- Use of interfering medications such as steroids or bisphosphonates
- Alcohol or drug abuse
- Heavy smoking (more than 10 cigarettes per day)
- Radiation therapy to head or neck within 5 years
- Untreated periodontitis
- Acute or chronic infections near teeth or tissues
- Severe skeletal discrepancies of the jaw
- Moderate to high parafunctional activity
- Absence of opposite teeth
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 - Procedure day
Participants receive complete arch restorations loaded immediately using a new stereophotogrammetry intraoral impression system as part of a full digital workflow.
1 visit (in-person)
Duration - 3 months
Participants are monitored for prosthetic success and any complications following the implementation.
Follow-up visits as scheduled during 3 months
Trial Site Locations
Total: 1 location
1
PTV
Roma, RM, Italy, 00133
Actively Recruiting
Research Team
P
Paolo Carosi, 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
1
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