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Comparing the Effectiveness of Two Bio-Ceramic Sealers in Treating Necrosed Teeth: A 6-Month Study Using CBCT-Advanced Imaging Technology

Phase 2
Conditions
Health Condition 1: K041- Necrosis of pulp
Registration Number
CTRI/2024/07/070005
Lead Sponsor
Dr Riddhi Vasa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Inclusion criteria

1.Systemically healthy patients (Category: American Society of Anesthesiologists Class 2 or less than 2) 25 between 18 – 65 years of age.

2.Maxillary or mandibular single rooted teeth diagnosed with Pulpal necrosis with symptomatic or asymptomatic apical periodontitis with lesions that show periapical radiolucency with (CBCTPAI) Score 323 will be included in the study.

3.Re-treatment cases with periapical lesions with CBCTPAI Score 3 will be included in the study.

4.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.

Exclusion Criteria

Exclusion criteria

1.Pregnant and lactating women will be excluded.

2 Patients having teeth with poor prognosis, open apices, internal/external resorption, fractured Roots or visibly cracked tooth, grade 3 mobility, severe periodontal bone loss will be excluded from the study

3.Patients having teeth with complex root canal morphology such as Calcified canals, extreme curvatures or anomalies will be excluded from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Healing of Periapical lesions is expected to be better than Cera seal bio-ceramic sealer in approximately 20 samplesTimepoint: Healing of periapical lesions will be assessed at baseline and after 6 months.
Secondary Outcome Measures
NameTimeMethod
PERIAPICAL HEALING WILL BE ASSESED ON CBCT AT BASELINE AND AFTER 6 MONTHSTimepoint: At baseline & after 6 months interval.
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