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Impacted Tooth With Immediate Implant Placement

Surgical Extraction of an Impacted Canine and Immediate Implant Placement: A Prosthetically Guided Digital Approach

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07456553
Acronym
ImmediateIMP
Enrollment
5
Registered
2026-03-06
Start date
2024-01-01
Completion date
2026-03-01
Last updated
2026-03-11

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

Conditions

Impacted Tooth

Keywords

Implantology, Prosthesis, Fixed Crown

Brief 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.

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.

Sponsors

University of Bari Aldo Moro
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

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 contraindication 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

* 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

Design outcomes

Primary

MeasureTime frameDescription
ISQAt implant insertion and after 3 monthsImplant stability quotient. ( 0 - 100)
Periimplant chart3 month after implant insertion, 1 year, 2 yearsProbing the implant in 6 site.

Countries

Italy

Contacts

PRINCIPAL_INVESTIGATORFrancesco Colacicco

University of Bari Aldo Moro

PRINCIPAL_INVESTIGATORGiuseppe D'Albis, Dr.

University of Bari Aldo Moro

STUDY_DIRECTORSaverio Capodiferro, Prof. Dr.

University of Bari Aldo Moro

STUDY_DIRECTORMassimo Corsalini, Prof. Dr.

University of Bari Aldo Moro

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026