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Comparative evaluation of two different regenerative materials in reconstruction of periodontal defects

Not Applicable
Conditions
Chronic Periodontitis.
Chronic pericoronitis Periodontitis: NOS complex simplex
Registration Number
IRCT2017022716141N3
Lead Sponsor
Vice chancellor for research of Dental School of Hamedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
45
Inclusion Criteria

At least have one intrabony periodontal defect.

Exclusion criteria: Smoking; Pregnancy; Systemic disease.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bone formation. Timepoint: 3 months after surgery. Method of measurement: Probing depth.;Bone formation. Timepoint: 3 month after surgery. Method of measurement: Radiography.
Secondary Outcome Measures
NameTimeMethod
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