To compare and evaluate the efficacy of natural and commercially available intracanal medicament using Cone Beam Computed Tomography.
Phase 2
- Conditions
- Health Condition 1: null- patients with endodontically involved teeth with periapical lesion greater than 3 mm
- Registration Number
- CTRI/2018/03/012782
- Lead Sponsor
- SRM Dental college Ramapuram
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age group between 18-45 yrs .
ASA I &II patients.
Subjects with periapical lesion of size greater than 3mm.
Patients will be selected based on the periapical index score with 3,4 and 5 preoperatively.
Teeth indicated for root canal treatment with periapical lesion.
Patient should not be under medication for past 8 hours.
Exclusion Criteria
Patients who are medically compromised or allergic to drugs or pollens.
Pregnant and lactating women.
Periodontally weak teeth.
Root caries.
Calcified rootcanals.
Retreatment cases.
Presence of Internal root resorption.
Blunderbuss canal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in size of periapical radiolucencyTimepoint: after 2 weeks
- Secondary Outcome Measures
Name Time Method Complete resolution of periapical radiolucency by evaluating after 1 year.Timepoint: at the end of 1 year