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Clinical Trials/NCT03578744
NCT03578744
Completed
Not Applicable

Efficacy of Platelet Rich Fibrin as a Graft and Membrane Versus Hyaluronic Acid and Amniotic Membrane in the Treatment of Mandibular Grade II and Grade III Furcation Defects- A Randomized Clinical Trial

Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre1 site in 1 country14 target enrollmentNovember 16, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Furcation Defects
Sponsor
Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre
Enrollment
14
Locations
1
Primary Endpoint
Radiological Parameters
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study is intended to compare the efficacy of platelet-rich fibrin as a graft and a membrane versus hyaluronic acid(Gengigel) and amniotic membrane in the treatment of mandibular grade II furcation defects.

Detailed Description

Platelet-rich fibrin is a fraction of plasma that provides a rich source of growth factors and may enhance the stabilization and revascularization of the flaps and grafts. Hyaluronic acid is a naturally occurring non-sulfated high molecular weight glycosaminoglycan that forms a critical component of the extracellular matrix and contributes significantly to tissue hydrodynamics, cell migration and proliferation. Hence its administration to periodontal wound sites could achieve beneficial effects in periodontal tissue regeneration. Amniotic membrane is being used for various regenerative procedures as it is a rich source of various collagen and non-collagen proteins such as laminin, fibronectin and proteoglycan.

Registry
clinicaltrials.gov
Start Date
November 16, 2017
End Date
October 30, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Boyeena Lavanya

Student

Panineeya Mahavidyalaya Institute of Dental Sciences & Research Centre

Eligibility Criteria

Inclusion Criteria

  • Grade II furcation involvement

Exclusion Criteria

  • Pregnant and lactating women,
  • Systemically compromised patients

Outcomes

Primary Outcomes

Radiological Parameters

Time Frame: Baseline and 9 months post surgery.

Amount of Bone fill in the furcation (Change in Bone level) to be measured by Cone Beam Computed Tomography(CBCT)

Secondary Outcomes

  • Clinical Parameter(Baseline and 9 months post surgery)

Study Sites (1)

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