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CompletedNCT07456553ImmediateIMPUpdated Mar 11, 2026

Impacted Tooth With Immediate Implant Placement

An interventional study of Implantology in Impacted Tooth, sponsored by University of Bari Aldo Moro. Completed at 1 site in Italy. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-11.

Sponsored by University of Bari Aldo Moro · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 2 months after the study started (first participant enrolled Jan 2024, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
5
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This is a prospective study, in which there are involved four clinical cases of surgical extraction of impacted maxillary canines followed by immediate implant placement and immediate screw-retained temporary crown using a full-digital workflow that included performing a CBCT, an intraoral scan, AI-assisted segmentation, a virtual wax-up, and the design of a surgical guide and a 30° angled abutment. Then, the follow-up lasting two years is performed to verify the functional and esthetical outcomes. The patients included in this report are part of an ongoing clinical trial, and the complete data set will be published separately upon study completion. The aims is to present clinical outcomes and synthesize evidence comparing placing implant to avoid buccal augmentation using angles abutments versus performing guided bone regeneration (GBR) to allow ideal implant placement with straight abutments, and to evaluate the risk of abutment screw loosening.

02

Conditions studied

  • Impacted Tooth

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Keywords

  • Implantology
  • Prosthesis
  • Fixed Crown
03

In context

Tooth, Impacted

122 studies on the registry are indexed under Tooth, Impacted; 15 are open to participants now.

This study's enrollment of 5 is below the median of 70 across 88 interventional studies indexed under Tooth, Impacted.

Browse Tooth, Impacted studies →

Lead sponsor

University of Bari Aldo Moro is the lead sponsor of 30 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Refuse Orthodontic treatments
  • Patients had to be healthy according to System of the American Society of Anesthesiology (ASA) and aged 18 years or older
  • No general medical condition representing a to implant therapy
  • minimum 2 missing teeth in the maxilla or mandible from the canine to the second molar
  • No periodontal disease (periodontal probing depth \<4 mm) or treated periodontitis
  • Good oral hygiene (full mouth plaque index\<25%)
  • Adequate control of inflammation (full mouth bleeding on probing\<25%)

Exclusion criteria

Exclusion Criteria:

  • smoking of more than 15 cigarettes a day
  • untreated periodontal disease
  • pregnancy or breastfeeding at date of inclusion
  • acute infections
  • keratinized mucosal tissue less than 2 mm
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
5 participants (actual)

Study arms

  • Experimental
    Patients with impacted tooth

    Patient with impacted Maxillary Canine.

    Procedure: Implantology

Interventions

  • ProcedureImplantology

    Following local anesthetic infiltration and a minimally invasive access, the atraumatic extraction of the impacted canine is performed, preserving the vestibular soft and bone tissues. The implant site is then prepared, and the implant is placed using the surgical guide, with the required insertion torque to achieve primary implant stability.

06

What researchers measure

Primary outcomes

  1. ISQ

    Implant stability quotient. ( 0 - 100)

    Time frame: At implant insertion and after 3 months

  2. Periimplant chart

    Probing the implant in 6 site.

    Time frame: 3 month after implant insertion, 1 year, 2 years

07

Study locations

1 site
  • Dr. Giuseppe D'Albis
    Bari, 70124, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07456553
Lead sponsor
University of Bari Aldo Moro
Responsible party
Giuseppe D'Albis (Principal Investigator, University of Bari Aldo Moro) — Principal investigator
First posted
Mar 6, 2026
Start date
Jan 1, 2024
Primary completion
Mar 1, 2026
Completion
Mar 1, 2026
Last update
Mar 11, 2026

Study contacts

Francesco Colacicco
principal investigator · University of Bari Aldo Moro
Giuseppe D'Albis, Dr.
principal investigator · University of Bari Aldo Moro
Saverio Capodiferro, Prof. Dr.
study director · University of Bari Aldo Moro
Massimo Corsalini, Prof. Dr.
study director · University of Bari Aldo Moro

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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