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Official title Oil Pulling Reduction
ClinicalTrials.gov ID: NCT07706647
What this study is testing
- What it's testing
- The goal of this study is to scientifically evaluate the efficacy of this oil pulling oral rinse in reducing dental plaque, gingival inflammation, gingival bleeding, and selectively reducing caries- and periodontal disease-associated bacteria compared to a marketed mouthwash and a placebo oral rinse
- You might receive a placebo (an inactive treatment) instead of the study drug.
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
You may be able to join if
- Adult people aged 18-70, that are in good health.
- Subject must have:
- Baseline gingival inflammation (MGI) score of at least 1.80.
- Baseline gingival bleeding (GBI) score of ≥ 1 on at least 20 sites.
- An overnight (12 to 18 hour abstention from any oral hygiene) dental plaque (mean) score greater than 0.6 according to the RMNPI Index.
You likely can't join if
- Current or history of oral cavity cancer or oropharyngeal cancer.
- Subject with destructive periodontal disease or those on antibiotic or anti-inflammatory drugs.
- Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body.
- Pregnant or nursing by subject report.
- Known allergic reaction to any of the study mouthwashes or any of their component.
- Any active condition, including but not limited to advanced periodontal disease or severe gingival recession, in the oral cavity at the discretion of...
See the full eligibility criteria
- Adult people aged 18-70, that are in good health.
- Subject must have:
- Baseline gingival inflammation (MGI) score of at least 1.80.
- Baseline gingival bleeding (GBI) score of ≥ 1 on at least 20 sites.
- An overnight (12 to 18 hour abstention from any oral hygiene) dental plaque (mean) score greater than 0.6 according to the RMNPI Index.
- Have a minimum of 20 'scorable' teeth (excluding 3rd molars).
- The people should understand the information provided about the investigative nature of the treatment, possible benefits and side effects. people will sign the Informed Consent Form.
- The people should be willing to comply with the study procedure and schedule, including the follow-up visits.
- Current or history of oral cavity cancer or oropharyngeal cancer.
- Subject with destructive periodontal disease or those on antibiotic or anti-inflammatory drugs.
- Pacemaker or internal defibrillator, or any other active electrical implant anywhere in the body.
- Pregnant or nursing by subject report.
- Known allergic reaction to any of the study mouthwashes or any of their component.
- Any active condition, including but not limited to advanced periodontal disease or severe gingival recession, in the oral cavity at the discretion of the investigator.
- Any surgery or recent dental procedure in the oral cavity within 3 months prior to treatment, or before complete healing.
- people that do not brush regularly.
- Any condition that might make it unsafe for the subject to participate in this study, at the discretion of the investigator.
- History of allergy or hypersensitivity to mouthwash ingredients
- Significant medical conditions, such as uncontrolled diabetes or immunosuppressive disorders
- Use of tobacco products, including cigarettes and smokeless tobacco
- Presence of orthodontic appliances, except for removable retainers
- Participation in another clinical trial within the last 30 days.
- Individuals unable to comply with study requirements, such as regular product use or scheduled visits.
- Habitual use of alcohol or drugs that may affect compliance or oral health
The study team makes the final eligibility decision.
Where it's taking place
- San Antonio, Texas, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
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. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include San Antonio, Texas, 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.