Fully digital workflow for immediate implants with same-day restoration
Official title: The Use of a Fully Digital Workflow in Immediate Implants With Immediate Restoration
Run by Proed, Torino, Italy · NCT07294820 · Data updated 2026-11-12
This project tests whether a fully digital workflow can give adults who need a single immediate implant with a same-day temporary crown the same implant survival, bone stability, and patient satisfaction as the standard analog approach.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 24 (estimated) |
| Sponsor | Proed, Torino, Italy Academic / other |
| Locations | 1 site (Turin, Piedmont) |
| Status | Recruiting |
| Started | January 27, 2026 |
| Main results expected | June 2028 |
| Study ends | June 2028 |
| Registry record updated | January 9, 2026 |
| Trial ID | NCT07294820 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults in good general health who need extraction and single-tooth replacement in the relevant tooth positions (immediate placement with immediate loading) and are willing to receive a same-day provisional crown are ideal candidates.
✕Probably not a fit
Patients with systemic health problems, inadequate bone at the extraction site, need for multiple adjacent implants, or who do not fit the single-tooth immediate placement criteria are unlikely to benefit from this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, single-arm observational study using Straumann BLX (BLC) implants and a full-digital workflow for immediate implant placement with immediate provisionalization. Pre-surgical planning combines cone-beam CT and intraoral scans to plan implant position and to produce a computer-guided surgical stent and a laboratory-prepared provisional crown. On the day of extraction, implants are placed using the guided approach and a temporary crown is delivered immediately; outcomes tracked include implant success and survival, marginal bone level changes, patient satisfaction by VAS, and procedure duration. The study builds on previously published case series of fully tapered BLX implants in the esthetic zone and records clinical and radiological measures over follow-up.
Why it matters
Potential benefit: If successful, this approach could let patients receive accurate, minimally invasive immediate implants with same-day temporaries and potentially improved aesthetics and shorter appointment times.
How similar studies have gone: Previous prospective case series using fully tapered BLX implants and digital planning in the esthetic zone have reported promising clinical and radiological results.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * adult systemically healthy patient requiring tooth extraction and single implant tooth replacement, from 1.5 to 2.5 Exclusion Criteria: * patients not fulfilling inclusion criteria
Where it's running
-
Studio Dottor Cardaropoli
Turin, Piedmont, Italy Recruiting
Study contacts
- Study coordinator: Daniele Franco Cardaropoli, dds
- Email: danielecardaropoli@gmail.com
- Phone: +393386688933
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.