Skip to main content
Clinical Trials/NCT03096210
NCT03096210
Completed
Not Applicable

Comparison of the Clinic, Radiographic and Histological Effects of Allograft and T-PRF (Titanium-Prepared Platelet Rich Fibrin) Materials in the Sinus Lifting Procedure. Preliminary Results From a Pilot Randomised Controlled Trial

Kırıkkale University0 sites18 target enrollmentMarch 11, 2013
ConditionsMaxillary Sinus

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Maxillary Sinus
Sponsor
Kırıkkale University
Enrollment
18
Primary Endpoint
Histological Examination
Status
Completed
Last Updated
5 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
March 11, 2013
End Date
March 2, 2015
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kırıkkale University
Responsible Party
Principal Investigator
Principal Investigator

Ebru Olgun Erdemir

Prof.Dr.

Kırıkkale University

Eligibility Criteria

Inclusion Criteria

  • Participants having been diagnosed to display a residual crest height of less than 5mm in posterior maxilla and non-smokers were included.

Exclusion Criteria

  • Participants with blood platelet disorders, infectious and metabolic diseases, ongoing chemotherapy or radiotherapy, history of chronic sinusitis associated with maxillary sinuses, taking any antibiotics and/or anti-inflammatory drugs were excluded.

Outcomes

Primary Outcomes

Histological Examination

Time Frame: At the first 4 and 6th months post surgery for the test and control groups, respectively.

Percentage (%) of new and old trabeculae formation post surgery

Secondary Outcomes

  • Implant stability measurements(Within the 3 months after implant surgery)
  • Radiological Examination(Within the first 4 and 6 months)

Similar Trials