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Study identifier: NCT07526129 Synced from ClinicalTrials.gov · July 29, 2026
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Impact of Alveolar Ridge Preservation on the Potential Need for Sinus Floor Elevation: A 10-year Retrospective Radiographical Study

Condition: Alveolar Bone Loss · Sinus Floor Augmentation · Sinus Pneumatization  ·  Sponsor: Saint-Joseph University

PhaseN/A
Planned participants130
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

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. These divisions will be conducted, according to: \- The residual bone height (RBH) which is the height in mm from the alveolar ridge crest to the lowest point of the maxillary sinus floor. The results of the proposed hypothesis are verified and interpreted after statistical analysis.

This description comes directly from the study's public registry record.

Talk to the study team

Nadine Chamas, Doctor of Dental Surgery  ·  +96176773326  ·  nadinechamas@outlook.com

Nadim Mokbel, DDS, MsC, PhD  ·  +9613256780  ·  nadim.mokbel@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Saint Joseph University of BeirutBeirut, Beirut, LebanonRecruiting

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Source record: clinicaltrials.gov/study/NCT07526129