New Stereophotogrammetry System to Capture Complete-arch Impression
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: FAST MAP.
- Who it may be relevant to
- Registry conditions: Prosthetic Complication, Prosthesis Failure, Dental. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
The Use of a New Stereophotogrammetry System to Capture Intra-operative Complete-arch Impression
Overview
Patients in need of complete arch restorations will be treated with dynamic navigation system. Once the implants are positioned, a new system of stereophotogrammetry will record the implant positions to capture a precise impression to deliver a fixed screw retained interim prosthesis
Interventions
- Device FAST MAP
Patients with complete arch restorations loaded immediately with a full digital workflow using stereophotogrammetry Intraoral impression
Primary outcome measures
- Prosthetic Success [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- Healthy patients aged ≥18 years
- Full mouth bleeding and full mouth plaque index lower than or equal to 25%
- Bone height for at least 10 mm long implants
- Bone width of at least 5 mm and 6 mm for narrow (NP 3.75/3.5 mm) and regular (RP 4.3 mm) implants, respectively
- Fresh extraction sockets with an intact buccal wall
- At least 4 and 5 mm of bone beyond the root apex in the mandible and maxilla
- Minimal insertion torque of 45 Ncm
Exclusion criteria
- General medical (American Society of Anesthesiologists, ASA, class III or IV) and/or psychiatric contraindications
- Pregnancy and/or breastfeeding
- Any interfering medication such as steroid therapy or bisphosphonate therapy
- Alcohol and/or drug abuse
- Heavy smoking (>10 cigarettes/day)
- Radiation therapy to head or neck region within 5 years
- Untreated periodontitis
- Acute and chronic infections of the adjacent tissues or natural dentition
- Severe maxillomandibular skeletal discrepancy
- High and moderate parafunctional activity
- Absence of opposite teeth
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Italy · 1 center
- PTV — Roma
Identifiers
NCT: NCT06745232 · FASTMAPPROSPECTIVE