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Clinical Trial Summary

This study was carried out to compare the outcome of sinus lift without grafting material, versus the use of moldable, self hardening calcium phosphate biomaterials with simultaneous implant placement.


Clinical Trial Description

This study was designed as a randomized controlled clinical trial, the study population consisted of 20 patients with missing maxillary posterior teeth and residual bone height 5-7mm. The sample was selected conveniently according to a list of inclusion and exclusion criteria, the participants were allocated randomly into two equal groups. All patients had sinus lift using piezosurgery device with simultaneous implant placement. In group I, blood clot was the only filling material. In group II, moldable, self-hardening calcium phosphate was the filling material. Clinical and radiographic evaluations were done through 6 months postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04214054
Study type Interventional
Source University of Alexandria
Contact
Status Completed
Phase N/A
Start date May 13, 2018
Completion date September 25, 2019

See also
  Status Clinical Trial Phase
Completed NCT04811768 - Lateral Bony Wall Repositioning in Maxillary Sinus Floor Augmentation Phase 4
Completed NCT05577520 - Maxillary Sinus Augmentation Using Different Size Bovine Bone Particles N/A
Completed NCT03184857 - Open Maxillary Sinus Augmentation Using Different Types of Bone Particles N/A
Completed NCT05735613 - Efficacy of Different Techniques of Crestal Sinus Lifting N/A