comparing the effect of two different materials on human dental pulp
Phase 3
- Conditions
- Human Pulp Regeneration.Dental drugs, topically applied
- Registration Number
- IRCT2013121415782N1
- Lead Sponsor
- self-sponsored by researchers in study
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
inclusion criteria: patients between 18 to 30 years old; patients that have at least 3 mature and intact third molars to be extracted; healthy periodontal condition
exclusion criteria: systemic diseases; medication intake
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical signs and symptoms (sensitivity to cold test and percussion). Timepoint: 1,3,7,14,21,28,35 and42 days after partial pulpotomy. Method of measurement: pulp vitality tests including thermal tests,Electric pulp test,pain, percussion, palpation,radiography.;Histologic pulp tissue evaluation including inflamation. Timepoint: day 42 after intervention. Method of measurement: light microscopic evaluation.;Histologic pulp tissue evaluation including dentin bridge formation. Timepoint: day 42 after intervention. Method of measurement: light microscopic evaluation.
- Secondary Outcome Measures
Name Time Method Histologic pulp tissue evaluation including pulp necrosis or abcess formation. Timepoint: after extraction(daye 42). Method of measurement: light microscopic evaluation.