Periodontitis Chronic Generalized Moderate Clinical Trial
Official title:
Biochemical Efficacy of Cymbopogon Citratus Gel as Local Drug Delivery Agent in Reducing Matrix Metalloproteinase-8 Levels Intra-crevicularly in the Treatment of Stage II Periodontitis: A Randomized Controlled Clinical Trial
Verified date | February 2022 |
Source | Alexandria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: Phytotherapeutics is widely used nowadays as an adjunct to scaling and root planing (SRP) to modulate inflammatory host response and eradicate microbes. Matrix metalloproteinase-8 (MMP-8) is associated with the onset of inflammation and considered an indicative biomarker to the severity of inflammatory response. Since MMP-8 can be used as a predictive biomarker for treatment response; our research aimed to investigate clinically the effectiveness of intra-pocket application of Cymbopogon citratus (lemongrass oil) gel and biochemically on MMP-8 levels in gingival crevicular fluid (GCF) of stage II periodontitis patients. Methods: A randomized controlled clinical trial was conducted on forty patients with stage II periodontitis, divided equally into two groups. Group-I (test) was managed by SRP with intra-pocket application of 2% lemongrass oil gel. Group-II (control) was managed by SRP with intra-pocket application of a placebo gel. Periodontal pocket depth (PPD) and clinical attachment loss (CAL) were measured for both groups, before treatment and twelve weeks after. Moreover, GCF was collected from both groups at baseline, one week, and twelve weeks after treatment. Then analysed by Enzyme-linked Assay (ELISA) technique.
Status | Completed |
Enrollment | 40 |
Est. completion date | December 4, 2021 |
Est. primary completion date | December 14, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 45 Years |
Eligibility | Inclusion Criteria: - systemically healthy individuals of both sexes having moderate periodontitis (stage II), CAL 3-4mm, with an age ranging from 25 to 45 years old. - patients with no history of previous periodontal therapy or taken any antibiotic therapy for the past six months Exclusion Criteria: - history of smoking, previous adverse reaction to the products (or similar products) used in this study, grade C category that has rapid rate of progression, and pregnant or lactating women |
Country | Name | City | State |
---|---|---|---|
Egypt | department of periodontology. Faculty of dentistry. Alexandria University | Alexandria |
Lead Sponsor | Collaborator |
---|---|
Souzy Kamal |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in periodontal pocket depth | the distance between the gingival margin and depth of probing | baseline and after 12 weeks | |
Primary | Change in clinical attachment loss | the distance between the CEJ and depth of probing | baseline and after 12 weeks | |
Primary | Change in Matrix metalloproteinase-8 level | Human Matrix metalloproteinase-8 level intracrevicularlly by collection of crevicular fluid sample | baseline and after 12 weeks |
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