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OpenTrials
Completed

NCT Number: NCT07175090

Evaluation of Coconut Oil Mouth Rinse on Periodontal Parameters

This study was based on testing a new natural mouthwash with coconut oil and xylitol as active agents to a placebo rinse on new periodontal parameters

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

University of Prishtina Dentistry School

Pristina, 10000, Kosovo

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Periodontitis grade I, II, III

Exclusion criteria

  • less than 20 teeth

Treatment and study plan

Coconut oil

Combination Product

The rinse is used three times a day during three weeks

Placebo

Other

Inactive ingredients with same taste and colour

Primary outcomes

  1. Improvement of gingival appearance

    Time frame: Three weeks of mouthrinse use

    The gingival index will be assessed before and after mouthrinse use

Secondary outcomes

  1. Gingival bleeding

    Time frame: Three weeks after mouthrinse use

    The presence of gingival bleeding will be assessed before and after mouthrinse use

Sponsors and collaborators

Lead sponsor

University of Pristina

Other

Registry information

Official study title

Evaluation of the Effectiveness of a Novel Coconut Oil Mouth Rinse on Periodontal Parameters: A Randomized Controlled Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Sep 16, 2025
Registry last updated
Sep 16, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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