BridgeMD
New treatment option for Gingivitis and Periodontal Diseases
Official title Evaluation of Toothbrush Bristles
ClinicalTrials.gov ID: NCT07306026
What this study is testing
- What it's testing
- The goal of this randomized clinical trial is to investigate two different types of toothbrush bristles. The main questions it aims to answer are the effects of two different bristle types on: how much plaque is on the teeth how deep the space is between gums and teeth how much gum and bone are attached to the teeth whether the gums bleed when checked if the gums get scratched or irritated Researchers will compare toothbrushes with tapered bristles to those with regular round bristles.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 70. Healthy volunteers may be eligible.
You may be able to join if
- Must have read, understood and signed an informed consent prior to being entered into the study.
- Must be 18 to 70 years of age, male or female.
- Have at least 20 natural or restored teeth, not including implants.
- Must have average Plaque Index of greater than 2 at screening.
- Must have more than 20% of pockets with bleeding on probing at screening.
You likely can't join if
- Physical limitations or restrictions that might preclude normal tooth brushing.
- Evidence of gross oral pathology
- Periodontal probing pocket depths (PPD) ≥ 5mm.
- Evidence of major soft tissue lesions or trauma at the baseline visit as determined by the examiner.
- Chronic disease with concomitant oral manifestations
- people who are currently undergoing, or require, extensive dental work, orthodontic treatment or periodontal surgery, or orthodontic treatment in the...
See the full eligibility criteria
- Must have read, understood and signed an informed consent prior to being entered into the study.
- Must be 18 to 70 years of age, male or female.
- Have at least 20 natural or restored teeth, not including implants.
- Must have average Plaque Index of greater than 2 at screening.
- Must have more than 20% of pockets with bleeding on probing at screening.
- Agree not to have a dental prophylaxis or any other elective, non-emergency dental procedures any time during the study.
- Agree to refrain from regular oral hygiene regimen for 24 hours and eating for 4 hours before the appointment in the study.
- Agree to abstain from the use of any dental products other than those provided in the study.
- Agree to comply with the conditions and schedule of the study.
- Physical limitations or restrictions that might preclude normal tooth brushing.
- Evidence of gross oral pathology
- Periodontal probing pocket depths (PPD) ≥ 5mm.
- Evidence of major soft tissue lesions or trauma at the baseline visit as determined by the examiner.
- Chronic disease with concomitant oral manifestations
- people who are currently undergoing, or require, extensive dental work, orthodontic treatment or periodontal surgery, or orthodontic treatment in the preceding 3 months
- Currently using bleaching trays
- Eating disorders
- Recent history of substance abuse
- Smoking \>10 cigarettes/day
- Participation in other clinical studies within 14 days of screening
- Pregnancy
The study team makes the final eligibility decision.
Where it's taking place
- Buffalo, New York, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 70 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Buffalo, New York, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.