Evaluation of the Effect of Oil Pulling
Study Details
Study Description
Brief Summary
The objectives of this study were to evaluate the inhibitory effect on plaque and the tooth discoloration associated with agents used in the chemical plaque control of oil pulling in comparison with chlorhexidine-containing mouthwash and water in a four-day plaque regrowth model.
One hundred dentistry students were included in this randomized, parallel-group, placebo-controlled clinical study. In this study, participants were divided into 5 equal groups: Group 1: Gargling with 0.2% chlorhexidine; Group 2: Oil pulling with coconut oil;
Group 3: Oil pulling with black cumin oil; Group 4: Oil pulling with terebinth oil; Group 4:
Gargling with distilled water. Participants were instructed to refrain from mechanical oral hygiene and rinse only with the allocated mouth rinse during the four-day period. The differences in plaque index, gingival index, and tooth discoloration were evaluated in the study.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Active Comparator: Chlorhexidine
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Drug: Chlorhexidine
Gargling with 10 mL 0.2% Chlorhexidine
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Experimental: Coconut Oil
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Other: Oil Pulling
In oil pulling therapy, a tablespoon of edible oil is placed in the mouth and swirled between the teeth for 15 to 20 minutes
|
Experimental: Black Cumin Oil
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Other: Oil Pulling
In oil pulling therapy, a tablespoon of edible oil is placed in the mouth and swirled between the teeth for 15 to 20 minutes
|
Experimental: Terebinth Oil
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Other: Oil Pulling
In oil pulling therapy, a tablespoon of edible oil is placed in the mouth and swirled between the teeth for 15 to 20 minutes
|
Placebo Comparator: Distilled Water
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Other: Distilled Water
Gargling with 10 mL distilled water
|
Outcome Measures
Primary Outcome Measures
- Dental Plaque [Day 4]
Plaque scores recorded by using the Quigley-Hein and Turesky plaque index (Q-H).
Secondary Outcome Measures
- Tooth Color [Day 1- Day 4]
The tooth color was determined with a digital spectrophotometer
Eligibility Criteria
Criteria
Inclusion Criteria:
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Without systemic disease,
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Had at least 24 teeth, and
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Without fixed or removable prostheses or orthodontic appliances
Exclusion Criteria:
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Individuals with a history of systemic or topical oral antimicrobial therapy use in the last 3 months
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Individuals with an allergy to any ingredient used in the study
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Smokers
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Pregnant or breastfeeding women
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Individuals with ≥2 mm gingival recession
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Ataturk University | Erzurum | None Selected | Turkey | 25240 |
Sponsors and Collaborators
- Ataturk University
Investigators
None specified.Study Documents (Full-Text)
More Information
Publications
None provided.- 8948