About this trial
This study aims to clinically assess this newly introduced Egyptian chemo-mechanical caries removal gel versus conventional drilling method . The concept of preserving healthy tooth structures and employing atraumatic restorative techniques during cavity preparation aligns with the principles of minimally invasive dentistry. This approach prioritizes patient comfort, reassurance, and fosters a positive perception of dental treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Open carious lesions with dentin involvement, but not involving the pulp in lower molars.
The access of the carious lesion has to be large enough to allow the penetration of the excavator.
Asymptomatic vital teeth, without clinical evidence of pulp, furcation, or periapical pathology.
Patients who sign informed consent.
Disqualifiers
Patients with spontaneous or elicited pain from caries.
Patients with systemic diseases.
Presence of intraoral/extraoral swellings.
Deep dental caries involving pulp.
Trial design
Parallel
Treatments tested in this trial
Cariemove
Procedure/SurgeryIt is a newly introduced Egyptian product. It consists of a transparent liquid containing 0.5% sodium hypochlorite, 0.1 M mixtures of three amino acids, leucine, lysine and glutamic acid.
Drilling using bur
Procedure/SurgeryRotary dental burs using high speed hand piece under water spray cooling system
Treatment groups
Trial outcomes
Primary outcomes
Level of anxiety and discomfort
Visual Analogue Scale from 0 to 10 (0 represents no pain and 10 represents the worst pain)
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: