Impact of Alveolar Ridge Preservation on the Potential Need for Sinus Floor Elevation: A 10-year Retrospective Radiographical Study
1 other identifier
observational
130
1 country
1
Brief Summary
This research aims to investigate the influence of alveolar ridge preservation, after extraction of maxillary posterior teeth, on the potential need of sinus floor augmentation procedures (that include lateral or crestal sinus augmentations). From peri-apical radiographs, maxillary posterior teeth will be divided into 4 groups according to the relationship of their apexes with the sinus. Then, the patients will be divided into 2 sub-groups: unassisted socket healing (only extraction) and ARP group (extraction + ARP) and their CBCT scans before implant placement will be collected. The CBCT scans should be at least 4 months post-extraction and ARP. Depending on the residual bone height, patients will be divided into 3 categories, according to the ABC classification:
- 1.In need of lateral sinus floor augmentation
- 2.In need of crestal sinus floor augmentation
- 3.No need for sinus floor augmentation, therefore, implant placement.
Trial Health
Trial Health Score
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participants targeted
Target at P50-P75 for all trials
Started Jan 2025
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2025
CompletedFirst Submitted
Initial submission to the registry
April 6, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 30, 2026
ExpectedApril 13, 2026
April 1, 2026
1.3 years
April 6, 2026
April 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Mid-ridge height in mm
on CBCT scans taken 4-12 months after extraction (with alveolar ridge preservation or not), mid ridge height will be measured in mm according to the ideal implant position; that will be planned on BlueSky Bio software
1 year
Secondary Outcomes (1)
need for either lateral sinus floor elevation, transcrestal sinus floor elevation or simple implant placement.
1 year
Study Arms (6)
Group 1: extraction + type 1
type 1 : the roots are not touching the maxillary sinus floor
group 2 : extraction + type 1 + ARP
type 1 : the roots are not touching the maxillary sinus floor + having underwent alveolar ridge preservation
group 3 : extraction + type 2
type 2 : the maxillary roots are touching the sinus floor
group 4 : extraction + type 2 + ARP
type 2 : the maxillary roots are touching the sinus floor + having underwent alveolar ridge preservation
group 5: extraction + type 3
type 3: the molar roots are protruding in the sinus
group 6 : extraction + type 3 + ARP
type 3: the molar roots are protruding in the sinus + underwent alveolar ridge preservation
Interventions
After extraction of posterior maxillary molars, teeth who underwent alveolar ridge preservation are included. This includes the extraction, curettage of the socket with a curette to eliminate any granulation tissue, and then the grafting of a bone material into the socket
Eligibility Criteria
Patients who underwent extraction of posterior maxillary molars at the Saint Joseph University of Beirut's dental center, having underwent alveolar ridge preservation or not.
You may qualify if:
- Patients aged ≥18 years.
- Patients who underwent alveolar ridge preservation after extraction of maxillary posterior teeth, as a test group.
- Patients who underwent extraction of maxillary posterior teeth with unassisted socket healing without alveolar ridge preservation as a control group.
You may not qualify if:
- The presence of a clinically symptomatic periapical radiolucency, acute abscesses, or chronic sinus tract, that may falsify the classification of posterior maxillary teeth on 2D radiographs.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Saint Joseph University of Beirut
Beirut, Beyrouth, 1000, Lebanon
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Target Duration
- 12 Months
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 6, 2026
First Posted
April 13, 2026
Study Start
January 1, 2025
Primary Completion
May 1, 2026
Study Completion (Estimated)
May 30, 2026
Last Updated
April 13, 2026
Record last verified: 2026-04