deltatrials
Recruiting INTERVENTIONAL NCT06533397

The Application of a Biphasic Calcium Sulfate Graft Material in Sinus Floor Elevation

Sponsor: Semmelweis University

Updated 4 times since 2024 Last updated: Apr 21, 2026 Started: Aug 24, 2024 Primary completion: Sep 1, 2026 Completion: Sep 1, 2031
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This observational or N/A phase trial investigates Alveolar Bone Loss and Edentulism Nos and is currently actively recruiting participants. Semmelweis University leads this study, which shows 4 recorded versions since 2024 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

~Aug 2024 – ~Sep 2024 · 31 days · monthly snapshot~Sep 2024 – ~Dec 2024 · 3 months · monthly snapshotRecruiting~Dec 2024 – ~Apr 2026 · 17 months · monthly snapshotRecruitingApr 28, 2026 – present · 2 months · daily APIRecruiting

Change History

4 versions recorded
  1. Apr 28, 2026 — Present [daily]

    Recruiting

    Phase: NANone

  2. Dec 2024 — Apr 2026 [monthly]

    Recruiting NA

  3. Sep 2024 — Dec 2024 [monthly]

    Recruiting NA

    Status: Not Yet RecruitingRecruiting

  4. Aug 2024 — Sep 2024 [monthly]

    Not Yet Recruiting NA

    First recorded

Eligibility Summary

Pneumatization of the maxillary sinus may lead to insufficient bone volume for dental implant placement in the edentulous posterior maxilla. Sinus floor elevation (SFE) surgery with the lateral window technique is a safe and predictable surgical intervention to restore bone height in the maxillary premolar and molar areas. According to the literature, several bone graft materials may be successfully applied for SFE surgery. There is a lack of evidence regarding the application of biphasic calcium sulfate (BCS) for SFE. The healing period following staged SFE is 2-9 months. The aim of this study is: * to evaluate the success of SFE surgery using BCS as graft material, * to compare the microarchitecture of the augmented bone depending on the healing period, * to evaluate the success of dental implants placed in the augmented bone and that of the prostheses delivered on the dental implants.

Contact Information

Sponsor contact:
  • Semmelweis University
Data source: ClinicalTrials.gov

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations