Coconut Oil Mouth Rinse for Periodontal Health
Coconut oil
+ Placebo
Chronic Disease+6
+ Stomatognathic Diseases
+ Mouth Diseases
Supportive Care Study
Summary
Study start date: June 1, 2024
Actual date on which the first participant was enrolled.This study examines the effectiveness of a new mouthwash containing coconut oil and xylitol to improve gum health. It is targeted at individuals who experience periodontal issues, which affect the gums and can lead to further dental problems if untreated. The aim is to determine if this natural mouthwash can provide better results than a placebo, which is a substance with no active ingredients. Finding a more effective mouth rinse could help people maintain better oral health naturally and without the use of chemical agents, potentially reducing the risk of gum disease. Participants in the study will use the coconut oil and xylitol mouthwash or a placebo rinse, which they swish around in their mouths as instructed. Researchers will evaluate the health of participants' gums by looking at new periodontal parameters to see if there are any improvements. The study does not mention specific risks or benefits beyond the general goal of assessing effectiveness, focusing instead on finding out whether this natural mouthwash can make a positive difference in gum health.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.120 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
Active ComparatorGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
University of Prishtina Dentistry School
Pristina, KosovoOpen University of Prishtina Dentistry School in Google Maps