COMPLETED

Clinical Study to Evaluate the Tooth Whitening Efficacy

Talk to us

Conditions

Whiteninghydrogen peroxide

Quick Navigation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Optic White 5%HP ActivShine TP vs Crest3D White TP (head-to-head whitening clinical) The objective of this study is to evaluate the tooth whitening efficacy of a Colgate toothpaste with 5% Hydrogen Peroxide and Fluoride compared to a toothpaste with 0% Hydrogen Peroxide and Fluoride over a one-week period.

Official Title

Clinical Study to Evaluate the Tooth Whitening Efficacy of a Colgate Toothpaste With 5% Hydrogen Peroxide and Fluoride Compared to a Toothpaste With 0% Hydrogen Peroxide and Fluoride Over a One-Week Period.

Quick Facts

Study Start:2025-04-25
Study Completion:2025-05-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06957249

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Signed Informed Consent Form;
  2. * Male and female subjects 18-70 years old, inclusive;
  3. * Good general health and good oral health based on the opinion of the study investigator;
  4. * All maxillary natural permanent anterior teeth (6-11) must be present;
  5. * Availability for the duration of the study;
  6. * Minimum average Vita Extended Bleachedguide 3D-Master shade score of 17 ≥ or darker.
  1. * Presence of orthodontic appliances and/or any anterior tooth with a prosthetic crown, veneer, or deemed non-vital;
  2. * Obvious signs of periodontal disease, rampant caries, or any condition that the dental examiner considers exclusionary from the study;
  3. * Five or more carious lesions requiring immediate care;
  4. * Concurrent participation in another clinical study;
  5. * Self-reported pregnant and/or lactating women;
  6. * History of allergies or sensitivity to tooth whitening products, hydrogen peroxide, personal care consumer products, or their ingredients;
  7. * Restorations on the teeth to be scored which may interfere with scoring procedures;
  8. * Have used a professional whitening product within one (1) year and/or had a dental prophylaxis (professional dental cleaning) within thirty (30) days prior to the start of the study

Contacts and Locations

Principal Investigator

John Gallob, DMD
PRINCIPAL_INVESTIGATOR
Consumer Research Consulting, LLC

Study Locations (Sites)

Consumer Research Consulting, LLC
Melbourne, Florida, 32940
United States

Collaborators and Investigators

Sponsor: Colgate Palmolive

  • John Gallob, DMD, PRINCIPAL_INVESTIGATOR, Consumer Research Consulting, LLC

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-04-25
Study Completion Date2025-05-03

Study Record Updates

Study Start Date2025-04-25
Study Completion Date2025-05-03

Terms related to this study

Keywords Provided by Researchers

  • hydrogen peroxide

Additional Relevant MeSH Terms

  • Whitening