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Recruiting NCT06745232

NCT06745232 New Stereophotogrammetry System to Capture Complete-arch Impression

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Clinical Trial Summary
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

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
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Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

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

Central Contact

Paolo Carosi, PhD

✉ paolo.carosi@alumni.uniroma2.eu

📞 327798699

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.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology