MedPath

Efficacy of connective tissue graft as a membrane and ABBM With and without PRP in treatment of intrabony defects

Not Applicable
Conditions
Alveolar vertical bony defects.
Registration Number
IRCT201104116167N1
Lead Sponsor
Dental Faculty,Islamic Azad University,Khorasgan ,Isfahan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

No amount of 25% or less plaque before surgery . Teeth with a mobility of less than 3 Miller . Endodontic treatment of teeth or vital teeth. . Patients with moderate to advanced chronic periodontitis and at least one pair of radiographic lesions in non-adjacent teeth, and vertically between the minimum level of attachment to the CEJ from the first phase of treatment is 5 mm. The depth of the defect during surgery is at least 3 mm. The vertical wall is 2 or 3 bone lesions. Exclusion criteria: 1. Systemic diseases 2. Pregnancy and breast feeding 3. The systemic use of antibiotics in the past three months 4. Abnormal platelet count before surgery in a month 5. Furcation involvement and grade 3 or 4 6. Other forms of chronic periodontitis periodontitis to 7. History of periodontal surgery in 6 Months

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pocket depth. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Clinical attachment level. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Free ginigival margin position. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.;Alveolar crest position. Timepoint: During and 6 months after. Method of measurement: Probe and Acrylic stent.;Defect depth to Stent. Timepoint: Before and 6 months after. Method of measurement: Probe and Acrylic stent.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath