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Comparison between two different root canal filling materials in patients with infection

Comparative Evaluation of clinical and radiographic outcome of root canal treatment obturated with bio-ceramic sealer and bio ceramic gutta-percha against Resin based sealer and gutta percha in patients with periapical radiolucency - A Randomized Clinical Study.

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043135
Enrollment
60
Registered
2022-06-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K047- Periapical abscess without sinus

Interventions

Intervention1: Bioceramic sealer and bioceramic gutta percha points: Endosequence bioceramic sealer and Endosequence bioceramic gutta percha points are biocompatible material which is to be used for o

Sponsors

Aishwarya Jain
Lead Sponsor

Eligibility

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 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
Radiographic outcome PAI scoreTimepoint: 3 and 6 months

Secondary

MeasureTime frame
Clinical outcomeTimepoint: 3 and 6 months

Countries

India

Contacts

Public ContactAishwarya Jain

KM Shah Denatl college and hospital

nshah7873@gmail.com9998994299

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026