To compare and evaluate the effectiveness of PRF with or without Osseograft in the treatment of intrabony defects in chronic periodontitis patients.
- Conditions
- Other Procedures,
- Registration Number
- CTRI/2021/07/035236
- Lead Sponsor
- Lishana Farnomi Ch Momin
- Brief Summary
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|Aims and objectives :
To compare and evaluate the effectiveness of Autologous Advanced PRF(A-PRF) with or without Bovine Derived Xenograft (Osseograft TM) in the treatment of intrabony defects in Chronic Periodontitis patients based on cliinical and radiographic parameters.
Materials and methods:
Fourty intrabony defects in which 40 patients were randomly divided into two different groups and were treated with group A (Ossegraft alone) and group B (Osseograft with A-PRF). Clinical parameters such as plaque index (PI), gingival index (GI), pocket probing depth (PPD), clinical attachment level (CAL) were assessed at baseline 1 month, 3 month and 6 month postoperatively; radiographic parameter such as percentage in bone fill (%BF) were calculated by using the computerized image analysis software.
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|Data collected will be entered into a computer and analyzed using the SPSS (Statistical Package for the Social Sciences) software. Results on continuous measurements will be presented on Mean ± SD and results on categorical measurements will be presented in Number (%).
Chi square analysis will be used to find the significance of study parameters on categorical scale. Student t test (two tailed, independent) will be used to find the significance of study parameters on continuous scale within and between two groups (Intra and Inter group analysis) on metric parameters.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 40
- 1.Patient in the age group between 30-60 years.
- Patient who are non smokers and do not consume tobacco in any form.
- Patients in good systemic health with no contraindications to periodontal surgery.
- Patients having pocket depth greater than 5mm, intraosseous defects greater than 3mm with radiographic evidence of vertical or angular bone loss in the affected sites.
- Involved teeth should be vital and asymptomatic.
- 1.) One-walled osseous defects.
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- Patients suffering from any systemic diseases judge to impair normal healing and immune-compromised patients.
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- Patients who had received any type of periodontal therapy for the past 6 months.
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- Patients taking immunosuppressant drugs like corticosteroids.
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- Patients with a known history of allergy to Doxycycline or Chlorhexidine or any other medicine used in the study.
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- Pregnant or lactating mothers.
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- Patients who were smokers or had tobacco in any other form.
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- Patients on anticoagulant therapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Plaque Index (P.I.) (Tureskey-Gilmore-Glickman Modification of Quigley Hein). At Baseline | After 1 month | After 3 month | After 6 month 2. Gingival Index (G.I.) (Loe and Silness, 1963) At Baseline | After 1 month | After 3 month | After 6 month 4. Clinical Attachment Level (CAL) At Baseline | After 1 month | After 3 month | After 6 month 3. Probing Pocket Depth (PPD) At Baseline | After 1 month | After 3 month | After 6 month
- Secondary Outcome Measures
Name Time Method The radiographic bone fill will be evaluated using Intraoral Periapical Radiographs of the surgical site Baseline-at baseline. immediately after the surgery and 6 month post-surgery
Trial Locations
- Locations (1)
Lishana Farnomi Ch Momin
🇮🇳Mumbai, MAHARASHTRA, India
Lishana Farnomi Ch Momin🇮🇳Mumbai, MAHARASHTRA, IndiaLishana Farnomi Ch MominPrincipal investigator8787681838cheranlishana@gmail.com