Skip to main content
OpenTrials
Completed

NCT Number: NCT07550491

Influence of Residual Bone Height on Marginal Bone Loss Around Implants Following Lateral Sinus Floor Augmentation With Deproteinized Bovine Bone Mineral

Data collection will be done on all patients who underwent a lateral maxillary sinus floor augmentation in the Faculty of Dental Medicine, both in the Periodontology Department and in the Oral Surgery Department.

Pre-surgical residual bone height will be measured on patients with a preoperative CBCT, and marginal bone loss will be measured in patients with a postoperative periapical radiograph that dates at least 3 years after implant placement.

In contrast to other studies who only associated between the presurgical residual bone height and implant survival / success rate, this study design takes a more in depth approach and measures the exact marginal bone loss on each implant. In addition, other factors will be taken into consideration (implant type, smoking status, diabetes status) to eliminate any confounding factors.

Completed

Looking for future studies?

Notify Me

Key information

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients who underwent a lateral maxillary sinus floor augmentation using deproteinated bovine bone matrix (DBBM) at the faculty before 2022.
  • Patients with pre-operative CBCT.
  • Patients with no visible sinus infection in the pre-operative CBCT.

Exclusion criteria

  • Patients who do not have a pre-operative CBCT.
  • Patients who do not have a post-operative orthogonal periapical radiograph that dates at least 3 years after implant placement.
  • Presence of inflammatory lesions at the surgical site (eg, sinusitis as assessed by CBCT).
  • Cases with sinus perforation.
  • History of radiation therapy in the head/neck region.
  • Use of bisphosphonates

Treatment and study plan

sinus lift using DBBM

Procedure

Sinus lift was performed to the patients, then after 9 months dental implants were placed.

Primary outcomes

  1. Marginal Bone Loss

    Time frame: at least 3 years after implant placement

    mesial and distal marginal bone loss were calculated from the implant platform to the first bone to implant contact

Sponsors and collaborators

Lead sponsor

Saint-Joseph University

Other

Registry information

Official study title

Influence of Residual Bone Height on Marginal Bone Loss Around Implants Following Lateral Sinus Floor Augmentation With Deproteinized Bovine Bone Mineral: A Retrospective Study Up to 12 Years.

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 24, 2026
Registry last updated
Apr 30, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.