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NCT06063980

Sinus Augmentation in the Posterior Maxillary Region: a Case Report of 0mm Bone Height.

Sinus Augmentation in the Posterior Maxillary Region: a Case Report of 0mm Bone
VNU University of Medicine and Pharmacy·ClinicalTrials.gov·procedureCompleted
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Study focus
Disease/Condition
Bone Resorption
Drug/Device/Intervention
Conventional sinus lift surgery
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
VNU University of Medicine and Pharmacy
Location
Hanoi, Vietnam
Timeline & enrollment
Phase
N/A
Start date
Mar 02, 2019
End date
May 01, 2023
Enrollment
2 participants
Primary outcome

Bone formation recorded after two-step-sinus-augmentation.

Summary

Sinus floor elevation (SFA) and GBR have been applied in the placement of dental implants in
 longstanding edentate posterior maxilla region. However, the number of study on the efficacy
 of these procedure on areas with 0mm bone height is limited. This case study aims to compare
 two cases of 0mm bone height in the posterior maxillae region with different handling
 procedure. In this article, two female patients in their 40s underwent maxillary sinus
 augmentation (sinus lifting) due to longstanding missing posterior maxillary molars with the
 bone of which area had resorbed entirely, leaving 0mm bone height. One patient went through
 conventional sinus augmentation while the other had a two-stage - sinus - lift procedure.
 Researchers compared the bone - volume induced between the two procedures.

ICD-10 classifications
OsteolysisPathological resorption of teethBone donorPostsurgical malabsorption osteoporosisPostsurgical malabsorption osteoporosis with pathological fracture
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06063980
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06063980 through Pure Global AI's free database. This phase not specified trial is sponsored by VNU University of Medicine and Pharmacy and is currently Completed. The study focuses on Bone Resorption. Target enrollment is 2 participants.

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