In-situ Clinical Trial Assessing Ability to Detect and Monitor Active Caries and Their Remineralization

Incisive Technologies Pty Ltd

Status

Active, not recruiting

Conditions

Dental Caries

Treatments

Device: BlueCheck

Study type

Interventional

Funder types

Industry

Other

Identifiers

NCT07100626

25-I-126

Details and patient eligibility

About

The goal of this clinical trial is to evaluate whether BlueCheck® can accurately detect and monitor early-stage dental caries (tooth decay) and their remineralization in adults. Participants will wear partial dentures with partially demineralized human enamel specimens. The main questions it aims to answer are:

Can BlueCheck® reliably detect early carious lesions with high sensitivity and specificity?
Does BlueCheck® visually reflect changes in remineralized enamel lesions?

BlueCheck® results will be compared against standard diagnostic methods (e.g., Nyvad criteria, Diagnodent readings, surface microhardness) to see if BlueCheck® provides an objective, accurate, and visual method of detecting and monitoring early-stage caries.

Participants will:

Wear a modified lower partial denture with four mounted enamel specimens for 28 days.
Use only the study-provided fluoride containing toothpaste
Attend weekly clinic visits for removal and laboratory analysis of one enamel specimen per week.
Undergo regular oral health checks and provide diary entries tracking brushing and any adverse events.

Enrollment

12 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

provide voluntary, written informed consent;
be between 18 and 85 years old;
understand and be willing, able and likely to comply with all study procedures and restrictions;
be wearing a removable mandibular partial denture with sufficient room to accommodate four (4) human enamel specimens (4 mm round) in their partial denture on both sides (two specimens on each side, bilateral partial denture) or one side (4 specimens on one side, unilateral partial denture)
be willing and capable of wearing their removable partial denture 24 hours a day for four (4), one-week treatment periods, maximum total duration four (4) weeks;
be willing to allow study personnel to drill specimen sites in the posterior section of one or both sides of their lower partial denture (teeth and/or buccal flange area below the teeth); and
be in good medical and dental health with no active caries or periodontal disease.
have a salivary flow rate in the range of normal values (unstimulated whole saliva flow rate ≥ 0.2 mL/min; gum base stimulated whole saliva flow rate ≥ 0.8 mL/min).

Exclusion criteria

currently be pregnant (self-reported), intending to become pregnant during the study period or breast feeding;
currently have any medical condition that could be expected to interfere with the subject's safety during the study period;
currently be taking antibiotics or have taken antibiotics in the two weeks prior to the beginning treatment;
known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients;
have participated in another clinical study or receipt of an investigational drug within 30 days of beginning treatment; or
be taking fluoride supplements, required to use a fluoride mouthrinse or have received a professional fluoride treatment in the two weeks preceding specimen placement.