Skip to main content
OpenTrials
Completed

NCT Number: NCT02430519

Benefits of Platelet Rich Fibrin In Mandibular Molar Furcation Defects

Background: Furcation is the bifurcation or trifurcation of a multirooted tooth. It is an area of complex anatomic morphology difficult to debride by routine periodontal instrumentation. Multiple approaches have been used in an effort to treat the furcation Choukroun's platelet-rich fibrin (PRF), a second generation platelet concentrate has biochemical components which have well known synergetic effects on healing processes. The present study was conducted to evaluate the effectiveness of autologous platelet-rich fibrin (PRF) in the treatment of mandibular molar Grade 2 furcation defects in comparison to allograft and guided tissue regeneration (GTR) membrane.

Completed

Looking for future studies?

Notify Me

Key information

About this study

ABSTRACT Background: Furcation is the bifurcation or trifurcation of a multirooted tooth. It is an area of complex anatomic morphology difficult to debride by routine periodontal instrumentation. Multiple approaches have been used in an effort to treat the furcation Choukroun's platelet-rich fibrin (PRF), a second generation platelet concentrate has biochemical components which have well known synergetic effects on healing processes. The present study was conducted to evaluate the effectiveness of autologous platelet-rich fibrin (PRF) in the treatment of mandibular molar Grade 2 furcation defects in comparison to allograft and guided tissue regeneration (GTR) membrane. MATERIALS AND METHODS: The study was designed as a randomized, prospective, parallel-arm, interventional clinical trial wherein 30 patients with periodontitis and grade II Mandibular furcation defects attending the Out Patient wing of the Department of Periodontics of a tertiary referral care hospital were equally divided into group A and group B. Patients in.Group A, were treated by the placement of PRF as a Graft and as a membrane at the surgical site , while in Group B, the defects were treated by the placement of Allograft and Healiguide collagen membrane. Plaque Index, Probing depth, Vertical clinical attachment level, Horizontal clinical attachment level, Gingival marginal level, and amount of bonefill using Radiovisiography were recorded at baseline and 9 months. Intra-group comparison of Mean scores between Group A and Group B was done using Paired t test and Inter-group comparison using independent sample t test. CONCLUSION Further studies evaluating the efficacy of PRF using a larger sample size should be performed to evaluate its true beneficial effects on long term basis in patients with mandibular molar Grade 2 furcation defects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • One or more sites showing grade II furcation involvement in mandibular molars, with Probing pocket depth ≥ 5mm
  • Vertical attachment level and horizontal level ≥3mm were considered.
  • Patients who were systemically healthy, with no history of endodontic and periodontal treatment for the last 6 months, and no antibiotic usage for the last 6 months were included in the study. Care was taken to ascertain that the samples taken for the study were not allergic to any drugs nor to the graft materials used.

Exclusion criteria

  • Patients with a history of diabetes, hypertension, on anticoagulant or steroid therapy (which could alter the effects of PRF), cardiac diseases, insufficient platelet counts and immunocompromised individuals were excluded from the study.
  • Care was taken to exclude pregnant women and lactating mothers, smokers, patients with previous history of graft placement in the experimental site, and importantly those patients who were unable to maintain good oral hygiene (PI Score ≥ 1.5).
  • If Grade II mobility was observed after phase I therapy in the experimental teeth, they were excluded

Treatment and study plan

Furcation treatment with PRF

Procedure

PRF Placed into the furcation after flap elevation and debridement

Other names: Furcation Management with Platelet rich fibrin

Furcation Treatment with Allograft and GTR

Procedure

Allograft and GTR placed into furcation after flap elevation and debridement

Other names: Furcation Management with DFDBM and Healiguide

allograft and guided tissue regeneration (GTR) membrane (DFDBM and Healiguide)

Device

autologous platelet-rich fibrin

Device

Primary outcomes

  1. Vertical clinical attacment level

    Time frame: 9 months Post treatment

    The Vertical clinical attachment level was assessed preoperatively and 9 months after surgery

  2. Horizontal clinical attachment level

    Time frame: 9 months Post treatment

    The horizontal clinical attachment level was assessed preoperatively and 9 months after surgery.

  3. Bone fill

    Time frame: 9 months Post treatment

    Bone fill was assessed radiographically and 9 months after surgery

Secondary outcomes

  1. Plaque Index

    Time frame: 9 Months Post treatment

    Plaque index was assessed preoperatively and 9 months after surgery

  2. Probing depth

    Time frame: 9 Months Post treatment

    Probing depth was assessed preoperatively and 9 months after surgery

  3. Gingival marginal level

    Time frame: 9 months post treatment

    Gingival marginal level was assessed preoperatively and 9 months after surgery

Sponsors and collaborators

Lead sponsor

Dr.Syed Asimuddin

Other

Registry information

Official study title

Effect of Autologous Platelet Rich Fibrin In Human Mandibular Molar Grade II Furcation Defects- A Clinical and Radiological Study

Acronym: PRFMMFD

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Apr 30, 2015
Registry last updated
Apr 7, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.