NCT06745232 New Stereophotogrammetry System to Capture Complete-arch Impression
| NCT ID | NCT06745232 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Rome Tor Vergata |
| Condition | Prosthetic Complication |
| Study Type | OBSERVATIONAL |
| Enrollment | 10 participants |
| Start Date | 2025-01-10 |
| Primary Completion | 2025-05-25 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 10 participants in total. It began in 2025-01-10 with a primary completion date of 2025-05-25.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
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
Eligibility Criteria
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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06745232 clinical trial?
This trial is open to participants of all sexes, studying Prosthetic Complication. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06745232 currently recruiting?
Yes, NCT06745232 is actively recruiting participants. Contact the research team at paolo.carosi@alumni.uniroma2.eu for enrollment information.
Where is the NCT06745232 trial being conducted?
This trial is being conducted at Roma, Italy.
Who is sponsoring the NCT06745232 clinical trial?
NCT06745232 is sponsored by University of Rome Tor Vergata. The trial plans to enroll 10 participants.