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A clinical trial to study the effects of two surgical procedures in chronic periodontitis patients.

Active, not recruiting
Conditions
Chronic periodontitis
Registration Number
CTRI/2016/10/007417
Lead Sponsor
Dr Harshal Pradip Patil
Brief Summary

The periodontal infection results from the subgingival colonization of periodontopathic bacteria. However, subgingival infection can cause anatomic changes in periodontal tissues ( i.e. Increased probing depth [PD], and furcation defects) that can produce local conditions that favor recurrence of disease. Periodontal treatment includes the surgical elimination of anatomic deformities by restoring lost supporting tissues. Periodontal regeneration refers to the reproduction or reconstitution of the lost or injured part. Guided tissue regeneration (GTR) is one technique with the most histologic documentation of periodontal regeneration in class II furcation defect. Various growth factors have been shown to accelerate the healing process. Platelet also releases growth factors which are natural biological mediators that regulate crucial cellular events involved in tissue repair. So platelet rich fibrin will provide growth factors and additionally the simplicity of procedure will help in treatment of class II furcation defect. The aim of this study is to evaluate the effectiveness of autologous platelet rich fibrin (PRF) membrane with open flap debridement (OFD) in the treatment of class II furcation defects compared to open flap debridement (OFD) alone

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
All
Target Recruitment
20
Inclusion Criteria
  • 1.Patients with age group 25-55 years 2.Both males and females 3.The presence of buccal class II furcation defects in endodontically vital, asymptomatic teeth with a radiolucency in the furcation area on an intraoral periapical radiograph with probing depth (PD)≥ 5 mm and horizontal PD ≥3 mm after phase I therapy (scaling and root planing).
  • 4.Absence of any local anatomical limitations 5.Patient willing for surgery and ready to give written consent.
Exclusion Criteria
  • 1.Systemic illness known to affect the outcomes of periodontal therapy 2.Individuals allergic to medications 3.Pregnant or lactating women 4.Patients using tobacco in any form 5.Individuals with unacceptable oral hygiene (plaque index [PI] >1.5).
  • 6.Teeth with interproximal intrabony defects, gingival recession, endodontic (pulpal) involvement, or mobility of tooth ≥Grade II will be excluded.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Probing depth, Clinical attachment level6 months
Secondary Outcome Measures
NameTimeMethod
Radiographic evaluation6 months

Trial Locations

Locations (1)

SMBT Dental College, Sangamner

🇮🇳

Ahmadnagar, MAHARASHTRA, India

SMBT Dental College, Sangamner
🇮🇳Ahmadnagar, MAHARASHTRA, India
Dr Harshal Pradip Patil
Principal investigator
9029762036
drharshalppatil@gmail.com

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