MedPath

A clinical study comparing outcome of regenerative root canal treatment with and without chitosan loaded triple antibiotic paste.

Phase 2
Registration Number
CTRI/2024/03/064482
Lead Sponsor
Dr.Asiya Mujawar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. patients in the age range of 18–30 years without systematic disease/allergic reactions

2. Nonvital single- rooted teeth (anterior or premolars) encasing 1 root canal with mature roots (closed apices) and a periapical lesion score =3 according to Ostravik et al.

Score 1: Normal periapical structure

Score 2: Small changes in bone structure

Score 3: Changes in bone structure with mineral loss

Score 4: Periodontitis with well-defined radiolucency

Score 5: Severe periodontitis with exacerbating factors

Exclusion Criteria

1. Medically compromised patients (with immunosuppressive/systemic diseases, patients on medications) - periodontologically compromised teeth.

2. Endodontically treated teeth

3. Teeth with periapical lesions more than 5 mm in diameter.

4. Patients who refuse to participate.

5. Anatomical variations leading to inability to reach the full working length.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the regenerative potential of pulp in necrotic mature teeth with and without chitosan loaded triple antibiotic paste.Timepoint: The outcome will be assessed at 6months and 1 year .
Secondary Outcome Measures
NameTimeMethod
Vitality of toothTimepoint: the vitality of the tooth will be assessed with electric pulp testing device after 6 months and 1 year of the treatment
© Copyright 2025. All Rights Reserved by MedPath