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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04382287
Other study ID # JRangel
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date November 20, 2019

Study information

Verified date May 2020
Source Universidad Autonoma de San Luis Potosí
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study aimed to compare the remineralisation capacity of white spot enamel lesions between two commercially available tooth pastes (Remin Pro and MI PASTE PLUS), applied at home twice a day on the anterior upper primary teeth by the patient and parents.


Description:

Objective: To evaluate and compare the clinical efficacy of Remin Pro® and MI Paste Plus® for the remineralisation of white spot lesions (WSL) on the enamel of primary teeth.

Methods: The selected design for this study was a randomised double-blind clinical trial based on CONSORT guidelines. Patients with at least one upper anterior primary tooth with a WSL on the enamel surface, with units of fluorescence (UF) ranged from 11-20 (evaluated with DIAGNOdent) were included in the study. Patients were randomly assigned to receive either the twice-daily at-home topical application of Remin Pro® or MI Paste Plus® (both as experimental pastes) or Colgate Total® (as control paste). The degree of remineralisation was quantified by the change in the number of UF from the baseline evaluation and at days 10 and 21. The difference between groups was statistically evaluated using ANCOVA and ANOVA techniques.


Recruitment information / eligibility

Status Completed
Enrollment 123
Est. completion date November 20, 2019
Est. primary completion date September 9, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years to 5 Years
Eligibility Inclusion Criteria:

- Young paediatric patients with at least one upper anterior primary tooth exhibiting one or several WSL on the smooth enamel surface.

- Attending the Paediatric Dentistry Postgraduate Program's Clinic

- Enamel lesions with units of fluorescence (UF) ranging from 11-20 as determined by DIAGNOdent

- Signed Informed Consent

Exclusion Criteria:

- History of hypersensitivity to any of the compounds of the pastes

- Enamel hypoplasia

- Compromising systemic diseases

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Remin Pro® and MI Paste Plus®
Te toothastes were applied at home twice a day over the six anterior upper primary teeth

Locations

Country Name City State
Mexico Faculty of Dentistry, Universidad Autónoma de san Luis Potosi San Luis Potosi

Sponsors (1)

Lead Sponsor Collaborator
Universidad Autonoma de San Luis Potosí

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Enamel remineralisation degree The remineralisation degree was quantified by the change in UF from the baseline (0 day) up to day 10 of twice-daily applications, by evaluation on the 10th day. 10 days
Primary Enamel remineralisation degree The remineralisation degree was quantified by the change in UF from the 10th day up to the 21st day, after twice-daily applications 21 days
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