Efficacy of Locally Delivered Coconut Oil in Management of Stage II and III Grade B Periodontitis. A Randomized Controlled Clinical Trial
topical application of coconut oil
+ scaling and debridement
Stomatognathic Diseases+1
+ Mouth Diseases
+ Periodontal Diseases
Treatment Study
Summary
Study start date: February 15, 2022
Actual date on which the first participant was enrolled.This study aims to explore how effective coconut oil is in treating a common gum disease called periodontitis, specifically in its moderate stages known as Stage II and III Grade B. Periodontitis is an inflammation of the tissues around the teeth, often caused by harmful bacterial buildup, affecting many people globally. The study is particularly important as it investigates whether adding coconut oil, known for its anti-inflammatory properties, to standard dental cleaning procedures can improve treatment outcomes. This approach could potentially offer a natural, effective way to enhance oral health care for those suffering from this condition. Participants in the study will undergo standard dental treatments, which include cleaning and removing plaque and tartar from the teeth. Some participants will also receive coconut oil applied directly to their gums as an additional treatment. The study will measure the effectiveness of this combined approach by observing changes in gum health and inflammation levels. The goal is to determine if the coconut oil enhances the effectiveness of traditional treatments, offering a new method to manage this common dental issue.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.34 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment 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.From 35 to 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers 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
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy 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