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Assessment of Marginal Bone Loss and Anterior Implant Stability in Immediate Versus Early Implant Placement

Assessment of Marginal Bone Loss and Anterior Implant Stability in Immediate Versus Early Implant Placement: A Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06985511
Enrollment
12
Registered
2025-05-22
Start date
2023-01-10
Completion date
2024-02-15
Last updated
2025-05-22

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

Conditions

Marginal Bone Loss

Brief summary

This study aims to determine the differences in implant stability and measurement of bone loss near implants between two different healing approaches used for teeth replacement in the front part of the upper jaw.

Interventions

PROCEDUREImmediate implant placement

Tooth extraction was performed atraumatically on one side, followed by immediate implant placement, right after extraction.

The tooth was extracted, and the implant was placed four weeks later (early placement).

Sponsors

Yasser Ahmed
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

split-mouth design

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Presence of unrestorable bilateral anterior teeth. * Harmonious gingival contour and thick gingival phenotype * Minimum 4 mm of apical bone and 2 mm of intact labial plate * Absence of periapical pathology

Exclusion criteria

* Systemic conditions affecting osseointegration or healing * Active oral infections or periodontal disease * Dehiscence or fenestration defects * Poor oral hygiene or heavy smoking

Design outcomes

Primary

MeasureTime frameDescription
Marginal Bone Lossup to 12 monthsCone beam computed tomography (CBCT) scans were obtained at the time of final restoration and post-placement. Measurements were made (in mm) from the implant platform to the most coronal bone level using OnDemand3D software. Each scan was oriented to align the implant with the axial plane. Measurements were performed by a single calibrated examiner to a precision of 0.01 mm.
Implant stabilityup to 12 monthsImplant Stability Quotient (ISQ) values were measured using Osstell. To ensure accuracy, the probe was positioned at a 90° angle and 3 mm above soft tissue level, as recommended in previous protocols. Osstell's patented technology uses the ISQ scale, with values ranging from 1 to 100, where higher values indicate greater stability

Countries

Lebanon

Outcome results

None listed

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