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Immediate Implant Placement: a Clinical and Radiographic Study on Hard and Soft Tissues Retraction at One Year.

Immediate Implant Placement: a Clinical and Radiographic Study on Hard and Soft Tissues Retraction at One Year.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05880771
Enrollment
30
Registered
2023-05-30
Start date
2021-01-01
Completion date
2024-11-30
Last updated
2025-05-16

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

Conditions

Guided Surgery, Immediate Implant Placement, Immediate Tamporization

Brief summary

This project consists of placing dental implants at extraction sites. Bone drilling and implant placement are performed using the flapless method with the use of a surgical guide allowing guided surgery. After implant placement, temporary teeth are immediately made and placed on the implants to guide the gingival contour. Bone and soft tissue retraction at the implanted sites are measured radiographically and digitally using surface scan superimposition over a 12-month period.

Interventions

OTHERImmediate Implant Placement

Tooth extraction followed by immediate implant placement. One group will have Allograft graft in the buccal gap, the other will have Xenograft graft.

Sponsors

Saint-Joseph University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
35 Years to 74 Years
Healthy volunteers
Yes

Inclusion criteria

* Absence of systemic or osseous disease that may impair peri-implant healing * Age ≥ 21 years * Acceptable oral hygiene * Presence of both adjacent teeth * Absence of acute infection in the treated area * Absence of periodontal pockets \> 3mm at the concerned site * Absence of pre-operative defect at the buccal bone wall (dehiscence or fenestration) * Per-operative integrity of the osseous and gingival structures (during tooth extraction) * Light or non-smoker (\<10 cigarettes per day)

Exclusion criteria

* Myocardial infarction within the past 6 months. * Poorly controlled diabetes (HBA1c \> 7.5%). * Coagulation disorders. * Radiotherapy to the head/neck area within the past two years. * Present or past treatment with intravenous bisphosphonates. * Immunocompromised patients. * Psychological or psychiatric problems. * Alcohol or drug abuse. * Poor oral hygiene and motivation (full mouth plaque score \> 30% and/or full mouth bleeding score \> 20%). * Uncontrolled periodontal disease.

Design outcomes

Primary

MeasureTime frameDescription
Hard tissue change by superimposing CBCT scans between 0 and 12 months using 3d slicer software12 monthsBuccal bone profil retraction after immediate implant placement using 2 different bone substitutes by comparing CBCT Dicom files at 0 and 12 months using 3d slicer software
Soft tissue change by superimposing surface intraoral scans between 0 and 12 months using 3d slicer software12 monthsSoft Tissue profil retraction after immediate implant placement using 2 different bone substitutes by superimposing STL files between 0 and 12 monts using 3d slicer software

Countries

Lebanon

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026