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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06384638
Other study ID # coconut periodontitis
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date February 15, 2022
Est. completion date February 9, 2024

Study information

Verified date April 2024
Source Misr University for Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Virgin Coconut Oil (VCO) is a vegetable oil extracted from coconut fleshcontains unsaturated fatty acids in the form of oleic acid and linoleic acid and flavonoids which function as anti-inflammatory. Periodontitis is an inflammatory disease of the periodontal tissues with a high prevalence worldwide. The main etiology of plaque periodontitis is biofilm containing colonies of pathogenic microorganisms. The aim of the study is to evaluate and compare the effect of scaling and root debridement alone versus the use of topically applied coconut oil as adjunctive to scaling and root debridement in treatment of Stage II and III Grade B periodontitis.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date February 9, 2024
Est. primary completion date January 16, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Years to 60 Years
Eligibility Inclusion Criteria: - patients age group >35 years without ant systemic disease - Willing to take part in the study. Patients with more than 16 natural teeth and have test teeth with both mesial and distal neighboring teeth with periodontitis with clinical attachment loss >3 mm and radiographic percentage of bone loss/age ranged between 0.25 to 1. - Patients with no history of allergies to coconut Exclusion Criteria: - smokers - pregnant - lactating women - Teeth with both endodontic-periodontal lesion.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
topical application of coconut oil
topical application of coconut oil
Other:
scaling and debridement
scaling and debridement

Locations

Country Name City State
Egypt Faculty of dentistry at MUST Giza

Sponsors (1)

Lead Sponsor Collaborator
Misr University for Science and Technology

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical parameters clinical attachment loss 3 months
Primary clinical parameters Probing depth 3 months
Secondary Biological parameters Tumor necrosis factor alpha (TNF- a) levels by using ELISA. 3 months
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