Comparison between two different root canal filling materials in patients with infectio
- Conditions
- Health Condition 1: K047- Periapical abscess without sinus
- Registration Number
- CTRI/2022/06/043135
- Lead Sponsor
- Aishwarya Jain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
1.Systemically healthy patients (Category: American Society of Anesthesiologists class 2 or less than 2) 25 between 18 – 65 years of age with maxillary or mandibular teeth diagnosed with symptomatic or asymptomatic apical periodontitis or acute exacerbation of chronic abscess will be included in the study.
2.Diagnosis will be based on clinical evaluation. Patients having positive response to tender on percussion and no response or extremely delayed response with electric pulp test will be included in the study.
3.Radiographic lesions that show periapical radiolucency or peri-radicular radiolucency with Periapical index (PAI) Score >3 will be included in the study.
4.Re-root canal treatment with periapical lesions with PAI Score >3 will be included in the study.
5.A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.
1.Pregnant and lactating women will be excluded.
2.Patients having uncontrolled diabetes, uncontrolled hypertension and immunocompromised will be excluded from the study.
3.Patients with history to any drug abuse will be excluded from the study.
4.Patients having teeth with poor prognosis, open apices, internal/external resorption, fractured roots or visibly cracked tooth, grade 3 mobility, severe periodontal bone loss with pocket depth of 6 mm or more than 6mm will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Radiographic outcome <br/ ><br>PAI scoreTimepoint: 3 and 6 months
- Secondary Outcome Measures
Name Time Method Clinical outcomeTimepoint: 3 and 6 months