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Completed

NCT Number: NCT02401360

A Study to Assess Clinical Gingivitis and Microbiome Following the Use of Multiple Oral Hygiene Products

This study assessed the efficacy of an oral hygiene regimen relative to a standard marketed toothpaste and manual toothbrush.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • give written informed consent prior to their participation;
  • be 18 to 65 years of age at the time of enrollment;
  • agree not to participate in any other oral/dental product studies;
  • agree to delay any elective dentistry (including a dental prophylaxis);
  • agree to refrain from the use of any non-study oral care products (including floss and mouthrinse) during the course of the study;
  • agree to return for the scheduled visits and follow study procedures;
  • be in good general health as determined by the investigator/designee based on a review of the health history/update for participation in the study;
  • have more than 10 bleeding sites at visits 1-3
  • Consistency of bleeding site number at baseline may be considered;
  • have a minimum of 18 natural teeth with facial and lingual scorable surfaces; and
  • refrain from performing any oral hygiene or consuming anything by mouth (except a small amount of water) at least 4 hours prior to their appointment.

Exclusion criteria

  • teeth that are grossly carious, fully crowned, extensively restored and have heavy dental calculus
  • antibiotic, anti-inflammatory or anti-coagulant therapy within two weeks of to the baseline exam
  • medical conditions that the investigator considers significant and that may compromise the evaluation of study results
  • currently participating in any other clinical trial
  • participated in a clinical trial for plaque/gingivitis within the previous 30 days
  • pregnant or lactating
  • orthodontic appliances or removable partial dentures
  • soft or hard tissue tumor of the oral cavity
  • advanced periodontal disease
  • history of hepatitis, diabetes, or other communicable diseases
  • history of rheumatic fever, heart murmur, mitral valve prolapse or other conditions requiring prophylactic antibiotic coverage prior to invasive dental procedures
  • history of significant adverse effects following the use of oral hygiene products such as toothpaste
  • oral pathoses that could interfere with compliance and/or examinations or that need treatment.

Treatment and study plan

China Crest® Pro-health 7 Complete Toothpaste

Drug

Crest® pro-health manual toothbrush Crest® pro-health gum protection rinse

China Crest® Cavity Protection Toothpaste

Drug

Crest® meliliangje manual toothbrush

Primary outcomes

  1. Gingivitis

    Time frame: Day 0

    Gingivitis was assessed according to the Gingival Bleeding Index

  2. Gingivitis

    Time frame: Day 3

    Gingivitis was assessed according to the Gingival Bleeding Index

  3. Gingivitis

    Time frame: Day 10

    Gingivitis was assessed according to the Gingival Bleeding Index

  4. Gingivitis

    Time frame: Day 24

    Gingivitis was assessed according to the Gingival Bleeding Index

Secondary outcomes

  1. Plaque Examination

    Time frame: Day 0

    The Modified Turesky Plaque Index was used to examine plaque.

  2. Plaque Examination

    Time frame: Day 3

    The Modified Turesky Plaque Index was used to examine plaque.

  3. Plaque Examination

    Time frame: Day 10

    The Modified Turesky Plaque Index was used to examine plaque.

  4. Plaque Examination

    Time frame: Day 24

    The Modified Turesky Plaque Index was used to examine plaque.

Sponsors and collaborators

Lead sponsor

Procter and Gamble

Industry

Registry information

Official study title

A Controlled Study to Assess Clinical Gingivitis and Microbiome Following the Use of Multiple Oral Hygiene Products

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Mar 27, 2015
Registry last updated
Oct 6, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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