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Clinical Trial Summary

This study will involve 14 patients with mandibular premolars indicated for extraction and immediate replacement. The patients will be randomly allocated into two groups and each patient will receive one implant. In Group A, a CGF membrane will be laid in the implant cavity. While in Group B, a PRF membrane will be laid in the implant cavity. Bone graft material will be applied to fill the empty parts of the socket. Resonance frequency measurement will be done using the OSTELL device intraoperatively, at the 1st week and after 3 months. Cone-beam computed tomography will be done preoperatively, immediately following surgery, and after 3 months


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05101954
Study type Interventional
Source Alexandria University
Contact
Status Completed
Phase N/A
Start date October 1, 2020
Completion date August 17, 2021

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