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Plaque Reduction Sesame Oil

The Plaque Reducing Efficacy of Oil Pulling With Sesame Oil. A Randomized-controlled Clinical Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06327841
Enrollment
40
Registered
2024-03-25
Start date
2022-06-21
Completion date
2022-08-18
Last updated
2024-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Plaque, Gingivitis, Oral Microbial Colonization

Brief summary

The goal of this clinical trials to learn about potential additives in reducing dental plaque. The main questions it aims to answer is: • is there a difference in the plaque reducing effect of oil pulling with sesame oil compared to rinsing with distilled water? Participants will rinse with 15 ml of their allocated liquid for 15 min every morning for 8 weeks. Researchers will compare sesame oil against distilled water to see if there is a difference in the plaque reducing effect.

Interventions

15min of oil pulling with 15ml sesame oil for 8 weeks

OTHERdistilled water

15min rinsing with 15ml distilled water for 8 weeks

Sponsors

Medical University Innsbruck
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* age ≥ 18 years * contractual capability * the presence of ≥ 10 teeth, * community periodontal index of treatment needs (CPITN) grade 1 or 2

Exclusion criteria

* missing consent * community periodontal index of treatment needs (CPITN) grade 0, 3 or 4 * pregnancy or breastfeeding * systemic diseases or conditions that are associated with an increased risk of infection or necessitate concomitant antibiotic therapy with dental treatment * mental and behavioral disorders that impede (verbal) communication * allergy against sesame(oil) * intake of antibiotics 6 months prior to or during study duration * intake of medication potentially influencing gingival inflammation or bleeding (e.g. anticoagulants, cortisone) * infectious diseases (e.g. HIV, hepatitis B or C) * fixed orthodontic appliances * ongoing oil pulling or mouth rinsing * adult guardianship * insufficient nasal breathing

Design outcomes

Primary

MeasureTime frame
Rustogi Modified Navy Plaque Index (RMNPI)first follow up after 4 weeks, full study duration 8 weeks

Secondary

MeasureTime frame
Gingival Index (GI)first follow up after 4 weeks, full study duration 8 weeks
microbial analysisfirst follow up after 4 weeks, full study duration 8 weeks
Oral Health Impact Profile (OHIP)first follow up after 4 weeks, full study duration 8 weeks
Interview halitosis, xerostomiafirst follow up after 4 weeks, full study duration 8 weeks

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026