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NOT YET RECRUITING
NCT07125846
NA

Efficacy of Bioactive Glass vs. Xenograft in Maxillary Sinus Augmentation

Sponsor: Suez Canal University

View on ClinicalTrials.gov

Summary

This randomized controlled study aims to evaluate the clinical, radiographic, and histologic efficacy of using bioactive glass bone graft (UNIGRAFT by Biomed Inc., USA) compared to a conventional xenograft in maxillary sinus augmentation procedures. A total of 20 patients classified as SA4 according to the Misch classification will be enrolled and randomly allocated into two groups. Outcomes will be assessed using Cone Beam Computed Tomography (CBCT) for vertical bone gain and, where applicable, histologic analysis. The study is conducted at the Faculty of Dentistry, Suez Canal University.

Official title: Clinical, Radiographic and Histologic Assessment of the Efficacy of Bioactive Glass as a Novel Grafting Material in Maxillary Sinus Floor Augmentation: A Randomized Controlled Study

Key Details

Gender

All

Age Range

20 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2025-10-15

Completion Date

2026-04-01

Last Updated

2025-08-15

Healthy Volunteers

No

Interventions

DEVICE

Bioactive Glass Bone Graft (UNIGRAFT)

A bioactive glass bone graft material (UNIGRAFT, Biomed Inc., USA) used for maxillary sinus floor augmentation via open sinus lift technique.

DEVICE

Xenograft Bone Graft (Bio-Oss)

A commercially available bovine-derived xenograft material (Bio-Oss, Geistlich Pharma) used for maxillary sinus floor augmentation via open sinus lift technique.