Health Condition 1: K044- Acute apical periodontitis of pulpal origin Health Condition 2: K045- Chronic apical periodontitis Health Condition 3: K041- Necrosis of pulp
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Endodontic-treated First molars 2.Absence of clinical signs and symptoms of periapical pathology 3.The presence of teeth in the proximal contact of the restoration 4.Teeth being in occlusion with antagonistic teeth 5. Patients who agreed to attend regular checks. 6. Minimum of one cusp with 3-mm thick. 7. Supragingival margins. 8. Good oral hygiene 9. Minimum of 18 years of age. 10.The absence of any systemic disease
Exclusion criteria
Exclusion criteria: 1. Participants who did not agree to sign the free informed consent form; 2. Tooth pain, unsatisfactory endodontic treatment, or signs of periapical lesions at the time of radiographic or clinical examination. 3. Unacceptable standard of oral hygiene or parafunctional habits 4. Severe periodontal problems 5. Pregnant women. 6. Volunteers who did not agree to follow-up visits. 7. Teeth with restorations, cracks, hypoplasia, or carious lesions on adjacent surfaces. 8. Participants undergoing orthodontic treatment. 9. Different dentists had carried out endodontic treatment. 10. The presence of any systemic disease
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| To compare the clinical performance of two different ceramic material used in fabrication of post-endodontic final restoration.Timepoint: 3 months, 6 months, 9 months, 1 year | — |
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this trial is to compare the clinical performance of post-endodontic full coverage and partial coverage restorations in restoring endodontically treated molars.Timepoint: 3 months, 6 months, 9 months, 1 year | — |
Countries
India
Contacts
All India Institute of Medical Sciences