Non-carious Cervical Lesions and Treatments

NACompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

August 1, 2017

Primary Completion Date

October 9, 2018

Study Completion Date

October 10, 2018

Conditions
Tooth Sensitivity
Interventions
DEVICE

Experimental: • Group LA

to apply Laser (780 nm and 70mW) at the cementum-enamel junction fat the teeth affected by sensitivity

DEVICE

Placebo Comparator: • Group LA-P

to apply Laser (780 nm and 70mW) at the cementum-enamel junction at the teeth affected by sensitivity with the laser device having no effective laser emission, only guided by light

OTHER

Experimental: • Group DE

to brush teeth with a blinded dentifrice with 0,45% of stannous fluoride and a soft-bristled manual toothbrush (Johnson \& Johnson®).

OTHER

Placebo Comparator: • Group DE-P

to brush teeth with a blinded dentifrice with 1500 ppm of available fluoride and a soft-bristled manual toothbrush (Johnson \& Johnson®).

OTHER

Experimental: • Group RGI

to apply a thin layer of resin based glass-ionomer product on the cervical surface of the affected teeth affected by sensitivity following the manufacturer instructions.

OTHER

Experimental: Group RX

to apply Adper Single Bond Plus Adhesive in accordance with the manufacturer instructions, at the teeth affected by sensitivity product for 20 seconds.

Trial Locations (1)

14040904

University of Sao Paulo -Ribeirao Preto Campus, Ribeirão Preto

All Listed Sponsors
lead

University of Sao Paulo

OTHER

NCT03403088 - Non-carious Cervical Lesions and Treatments | Biotech Hunter | Biotech Hunter