root canal therapy
Phase 3
- Conditions
- pulpectomy.
- Registration Number
- IRCT2013112615558N1
- Lead Sponsor
- Vice chancellor for research of Mashhad university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
children with no systemic disease;
mandibular second primary molar tooth with periradicular radiolucency
Exclusion criteria:
children with systemic and immunosuppressed diseases and sensitive to antibiotic drugs;
hyperemic pulp
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical success. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: examination and observation, expression by pateint.;Radiographic success. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: radiographic feature.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: expression by patient.;Fistula. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: examination and observation.;Abscess. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: examination and observation.;Tenderness to percussion. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: examination and observation.;New radiolucent lesion. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: radiographic feature.;Change in primary lesion. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: radiographic feature.;Internal or external resorption. Timepoint: 2 and 6 and 12 months after intervention. Method of measurement: radiographic feature.