Titanium-Prepared Platelet Rich Fibrin in the Sinus Lifting Procedure

Status Completed

Clinical Trial Summary

This study evaluates the radiographic, histological and clinical comparisons of the completely autologous T-PRF or allograft effectiveness at the maxillary sinus elevation procedure.

Clinical Trial Description

Participants randomly divided into 2 groups and the test group had a Schneiderian membrane elevation with using balloon lifting technique and after that sinus was filled with T-PRF produced from the patients' blood and 4 months waiting period has been entered. At the end of the 4th month, the bone samples were received from the implant slots and sent to histological evaluation. After 3 months, implant stability was measured and recorded. In the control group, the same procedures were followed and sinus was filled with only allograft. Waiting period was changed to 6 months for this group. ;

Study Design

Related Conditions & MeSH terms

Maxillary Sinus

Clinical Trial Details

NCT number	NCT03096210
Study type	Interventional
Source	Kirikkale University
Contact
Status	Completed
Phase	N/A
Start date	March 11, 2013
Completion date	March 2, 2015

View Details

See also
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