Toothpaste with Chitosan for Reducing Gum Bleeding

Clinical Investigation of Bleeding Reduction Efficacy on Toothpaste Containing 1.05% Chitosan

Not applicable Interventional Colgate Palmolive · NCT06955871

This study tests if a new toothpaste with Chitosan can help people with gum bleeding more than regular fluoride toothpaste or a bicarbonate toothpaste.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment150 (estimated)
Ages18 Years to 70 Years
SexAll
SponsorColgate Palmolive Industry-sponsored
Locations1 site (Chengdu, Sichuan)
Trial IDNCT06955871 on ClinicalTrials.gov

What this trial studies

This clinical investigation evaluates the effectiveness of a toothpaste containing 1.05% Chitosan in reducing gum bleeding compared to a standard fluoride toothpaste and a toothpaste with 67% bicarbonate. Participants will be assessed for their gum health and bleeding during routine brushing over the study duration. The study aims to determine if the Chitosan toothpaste provides superior results in managing gingivitis and bleeding gums.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18-70 with at least 20 natural teeth and a Modified Gingival Index score of 2.5 or higher.

Not a fit: Patients with severe systemic health issues or those who are pregnant or lactating may not benefit from this study.

Why it matters

Potential benefit: If successful, this toothpaste could significantly improve oral health by reducing gum bleeding and gingivitis symptoms.

How similar studies have performed: Previous studies have shown promising results with similar oral health interventions, suggesting potential efficacy for this approach.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male or female subjects, aged 18-70, inclusive.
2. Availability for the duration of the study.
3. Ability to understand and willingness to read, and sign the Informed Consent Form after the nature of the study has been fully explained to them.
4. Willingness to comply with all study procedures and clinical examination schedules.
5. Good general health (absence of any condition that, in the opinion of the study examiner, might constitute a risk to the subject while participating in the study. Examples include heart problems, valve/hip replacements etc).
6. Presence of a minimum of 20 natural teeth (excluding third molars) with facial and lingual scoreable surfaces.
7. Have a mean Modified Gingival Index (Lobene) ≥ 2.5 at screening.
8. Subjects reporting bleeding while routine toothbrushing.

Exclusion Criteria:

1. Pregnant or lactating.
2. Use of tobacco products.
3. History of alcohol or drug abuse.
4. Medical condition (especially, heart or liver problems, bleeding disorders, blood dyscrasias) or any current usage of medication that the investigator considers may compromise the subject safety, as well as, the quality of the study results.
5. Medical condition which requires pre-medication prior to dental visits/procedures.
6. History of allergy to oral hygiene products.
7. Use of anti-inflammatory, immunosuppressive, antimicrobial or anticoagulant drugs or antibiotics in the 30 days prior to the start of the study and during the course of the study.
8. Ongoing use of medications known to affect the gingival tissues (i.e. calcium channel blockers, phenytoin, cyclosporine).
9. Presence of orthodontic bands or removable partial denture(s).
10. Tumor (s) of the soft or hard tissues of the oral cavity.
11. Five or more carious lesions requiring immediate restorative treatment.
12. More than 2 periodontal pockets (\>4mm deep) with bleeding on probing.
13. Any gingival condition like hyperplasia or overgrowth, that would cause difficulty in clinical assessment.
14. Participation in any other clinical study with an oral care indication or test panel within 30 days prior to the start of the study.
15. Existing medical condition which prohibits the subject from not eating or drinking for periods of up to 2 hours.

Where this trial is running

Chengdu, Sichuan

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Bleeding GumGingivitis
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.