Carious Tissue Selective Removal on Permanent Posterior Teeth.

Juan Gonzalo Olivieri111 enrolled

Overview

This study is a prospective randomized controlled study of patients who come to the University. The aim is to evaluate the success rate of selective removal of carious tissue in deep lesions of posterior teeth. Three different materials will be used as liners (VitreBond ™Plus, BioDentine™, and Theracal™ LC). Post-operative pain, clinical, and radiographic success will be evaluated at one, two, and five-year follow-up. The null hypothesis is that there will be no statistically significant differences in rates of successful treatment with the three materials used.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

111

Conditions

Dental Caries Dental Materials

Interventions

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients that demonstrate understanding of the study and willingness to participate as evidenced by signing the voluntary informed consent and received a signed and dated copy of the informed consent form. * Understands and is willing to comply with all study procedures and restrictions. * Not presence of clinically significant and relevant abnormalities of clinical history or oral examination. * Diagnosis of normal pulp or reversible pulpitis. * No presence of periapical periodontitis * Posterior teeth Exclusion Criteria: General: Patients with systemic diseases, diabetes, immunocompromised and pregnant women, or any clinically significant or relevant oral abnormalities. Specific: Impossibility of restoration, diagnosis of irreversible pulpitis or necrosis, preoperative pain

Outcomes

Primary Outcomes

Clinical post-operative pain

VAS score of patient' level of pain, from no pain to extreme pain

Time frame: Immediately post-treatment

Clinical post-operative pain

VAS score of patient' level of pain, from no pain to extreme pain

Time frame: 8 hours post-treatment

Clinical post-operative pain

VAS score of patient' level of pain, from no pain to extreme pain

Time frame: 24 hours post-treatment

Clinical post-operative pain

VAS score of patient' level of pain, from no pain to extreme pain

Time frame: 48 hours post-treatment

Clinical signs or symptoms of pulp or periapical disease

Absence/presence of clinical signs or symptoms of pulp or periapical disease

Time frame: 1 year

Clinical signs or symptoms of pulp or periapical disease

Absence/presence of clinical signs or symptoms of pulp or periapical disease

Time frame: 2 years

Clinical signs or symptoms of pulp or periapical disease

Absence/presence of clinical signs or symptoms of pulp or periapical disease

Time frame: 5 years

Radiographic signs of periapical disease

Absence/presence of radiographic apical periodontitis

Time frame: 1 year

Radiographic signs of periapical disease

Absence/presence of radiographic apical periodontitis

Time frame: 2 years

Radiographic signs of periapical disease

Absence/presence of radiographic apical periodontitis

Time frame: 4 years

Carious Tissue Selective Removal on Permanent Posterior Teeth.

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes