Actively Recruiting

Phase 1
Phase 2
Age: 12Years - 18Years
All Genders
Healthy Volunteers
NCT05852145

Oral Changes With Caloric and no Caloric Sweeteners

Led by Hospital Infantil de Mexico Federico Gomez · Updated on 2025-10-09

52

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of this clinical trial is to compare the effect that the intake of beverages without sweeteners, added with non-caloric sweeteners (stevioside) and caloric sweeteners (sucrose) on oral pH and dental biofilm microbiome in Mexican adolescents. Participants will drink on different occasions a beverage without sweetener, a beverage added with stevioside or a beverage added with sucrose. The researchers will compare the changes that each one causes in salivary pH, dental biofilm pH, dental biofilm bacterial proliferation and dental biofilm microbiome.

CONDITIONS

Official Title

Oral Changes With Caloric and no Caloric Sweeteners

Who Can Participate

Age: 12Years - 18Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Habitual consumption of soft drinks
  • Decayed, Missing, and Filled Teeth (DMF) index of at least 3 (visible caries without drying the tooth)
  • Agree to participate and sign informed consent
  • Parents agree and sign informed consent
  • Any nutritional condition
Not Eligible

You will not qualify if you...

  • Undergoing orthodontic treatment
  • Received topical fluoride applications in the last 3 months
  • Motor disability interfering with tooth brushing
  • Xerostomia (dry mouth)
  • Taking antibiotics during the study period
  • Having periodontal infections

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hospital Infantil de México Federico Gomez

Mexico City, Cuahutemoc, Mexico, 06720

Actively Recruiting

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Research Team

A

América L Miranda, PhD

CONTACT

G

Guadalupe C Barajas, MsC

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

3

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