Selective Removal Technique With or Without a Bioactive Material for Deep Caries Lesions

Not Applicable

Recruiting

• Conditions: Deep Caries
• Interventions: Procedure: Selective removal to soft dentin, Biodentine; Procedure: Selective removal to soft dentin, No Base

• Registration Number: NCT04743219
• Lead Sponsor: Universidad Rey Juan Carlos

Brief Summary

Objectives: To evaluate and compare clinical and radiographic success of the selective removal to soft dentine technique in one step using calcium silicate cement (Biodentine) vs. no indirect pulp capping material in patients with deep caries lesions in mature permanent posterior teeth with normal or reversible pulpitis after a 2 year follow-up. Evaluate the integrity of the resin composite restorations using FDI criteria.

Material and methods: selective removal to soft dentine in one visit will be performed in 104 blinded patients that will be randomly allocated into 2 study arms, 52 patients will constitute the Biodentine group and 52 the No material group. Clinical examination will be performed to obtain pre-, intra- and postoperative data, including vitality test results, periapical status and risk of caries of the patients. Periapical and bitewing radiographs will be taken before treatment (T-0), at 1 month (T-1), 6 months (T-2), 12 months (T-3) and 24 months (T-4). Restorations will be assessed using the FDI criteria at the same follow up periods.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-02-01
• Study First Submitted: 2021-02-01
• Study First Submitted QC: 2021-02-05
• Study First Posted: 2021-02-08
• Status Verified: 2022-11
• Last Update Submitted: 2022-11-18
• Last Update Posted: 2022-11-21
• Primary Completion: 2025-03-01
• Study Completion: 2025-04-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 104

Inclusion Criteria

• Patients older than 15 years.
• Parents or guardians of patients under 18 years of age, but over 15 years of age, and patients over 18 years of age who demonstrate understanding of the study and willingness to participate as evidenced by signing the voluntary informed consent and who receive a signed and dated copy of the informed consent form.
• Occlusal or occlusal-proximal caries lesions, Class I or Class II, in molars or premolars with enamel margins and affecting maximum one proximal wall.
• Molar or premolar with deep caries lesion, involving equal to or greater than two thirds of dentin in depth, with a radiographically identifiable band of healthy dentin separating the pulp chamber roof from the caries lesion.
• Normal response to tests of sensitivity (normal pulp) or discomfort when cold stimulus is applied that disappears in a couple of seconds after the elimination of the stimulus (reversible pulpitits).
• Teeth with negative percussion.

Exclusion Criteria

• Patients immunosuppressed or with severe systemic diseases.
• Teeth with root or cervical resorption.
• Teeth with obliteration of the pulp chamber.
• Periapical or furcal radiolucency.
• Patients with periodontal disease.
• Patients with spontaneous acute pain, prolonged excruciating pain and / or pain that disturbs night sleep.
• Patients who have an allergy to any of the materials used in the treatment.
• Patients with caries lesions that during the treatment of their removal a pulp exposure is performed.
• Patients with inadequate initial radiographs for analysis.
• Evidence of pre-cancerous or cancerous lesions.
• Patients who have taken antibiotics in the last two weeks.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Biodentine Group	Selective removal to soft dentin, Biodentine	Biodentine group: patients with mature permanent posterior teeth with deep caries lesions treated with the selective removal technique to soft dentin with Biodentine as indirect pulp capping material before placement of a definitive direct composite resin restoration.
No base Group	Selective removal to soft dentin, No Base	The experimental group or No Base group: patients with mature permanent posterior teeth with deep caries lesions treated with the selective removal technique to soft dentin without the placement of a bioactive material as a base and restored directly with a definitive direct composite resin restoration.

Primary Outcome Measures

Name	Time	Method
Clinical success	2 years	Clinical success is defined as healthy pulp, determined by a normal positive not prolonged response in the clinical examination to the cold test and the electrical test, negative response to percussion, absence of symptoms or signs of infection (abscess, fistula, swelling or inflammation) and absence of spontaneous pain.

Secondary Outcome Measures

Name	Time	Method
Radiographic success	2 years	Radiographic success is defined as the absence of widening of the periodontal ligament space (twice the equivalent of the adjacent healthy tooth) and the absence of a periapical or furcal lesion on radiographic examination. A periapical lesion is considered to be a radiolucency associated with the radiographic apex of the root of a size greater than twice the width of the periodontal ligament space.

Trial Locations

Locations (1)

Universidad Rey Juan Carlos; 🇪🇸 Alcorcón, Madrid, Spain