New Stereophotogrammetry System to Capture Complete-arch Impression

The Use of a New Stereophotogrammetry System to Capture Intra-operative Complete-arch Impression

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06745232

Enrollment

Registered

2024-12-20

Start date

2025-01-10

Completion date

2025-08-01

Last updated

2025-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prosthesis Failure, Dental, Prosthetic Complication

Keywords

fixed prosthesis, stereophotogrammetry, immediate loading

Brief summary

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

DEVICEFAST MAP

Patients with complete arch restorations loaded immediately with a full digital workflow using stereophotogrammetry Intraoral impression

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

1. Healthy patients aged ≥18 years 2. Full mouth bleeding and full mouth plaque index lower than or equal to 25% 3. Bone height for at least 10 mm long implants 4. 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 5. Fresh extraction sockets with an intact buccal wall 6. At least 4 and 5 mm of bone beyond the root apex in the mandible and maxilla 7. Minimal insertion torque of 45 Ncm

Exclusion criteria

1. General medical (American Society of Anesthesiologists, ASA, class III or IV) and/or psychiatric contraindications 2. Pregnancy and/or breastfeeding 3. Any interfering medication such as steroid therapy or bisphosphonate therapy 4. Alcohol and/or drug abuse 5. Heavy smoking (\>10 cigarettes/day) 6. Radiation therapy to head or neck region within 5 years 7. Untreated periodontitis 8. Acute and chronic infections of the adjacent tissues or natural dentition 9. Severe maxillomandibular skeletal discrepancy 10. High and moderate parafunctional activity 11. Absence of opposite teeth

Design outcomes

Primary

Measure	Time frame	Description
Prosthetic Success	3 months	Prosthetic success of interim prosthesis in term of passivity and tissues adaptability

Countries

Italy

Contacts

Primary ContactPaolo Carosi, PhD

paolo.carosi@alumni.uniroma2.eu327798699

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026