Skip to content

Effect of Omega 3 on Periodontitis in Postmenopausal Women

Effect of Omega 3 Fatty Acids on Chronic Periodontitis Patients in Postmenopausal Women: A Randomized Controlled Clinical Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02764879
Enrollment
50
Registered
2016-05-06
Start date
2014-07-31
Completion date
2015-06-30
Last updated
2016-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Periodontitis

Keywords

Omega 3 fatty acids, Root planning, chronic periodontitis

Brief summary

The study was aimed to investigating changes in periodontal parameters and superoxide dismutase activity after root surface debridement with and without Omega 3 fatty acids (ω-3 FAs) supplementation in postmenopausal women. Adjunctive Omega 3 fatty acids supplements reduce periodontal inflammation and improve the status of systemic enzymatic antioxidants in postmenopausal women.

Detailed description

Fifty postmenopausal women with chronic periodontitis were divided randomly into two groups: Group 1 (n=25) were provided periodontal treatment in the form of scaling and root planing (SRP) plus placebo soft gelatin capsules while group 2 (n=25): patients were received SRP along with systemic administration of Omega 3 fatty acids. Clinical parameters and superoxide dismutase (SOD) activity in the gingival crevicular fluid were recorded at baseline, 3 and 6 months after therapy. The research has been conducted between July 2014 and June 2015. By the end of the study period, the Omega 3 treated group was able to achieve a greater mean probing pocket depth reduction, mean gain in clinical attachment level, as well as greater increase in SOD activity (P\<0.01) compared to SRP alone.

Interventions

DIETARY_SUPPLEMENTOmega 3 fatty acids

omega3 received 2 times daily-for 6 months

PROCEDUREscaling and root planing
OTHERplacebo soft gelatin capsules

placebo soft gelatin capsules received 2 times daily-for 6 months

Sponsors

October 6 University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Postmenopausal women with generalized chronic periodontitis (clinical attachment loss more than 30% of the teeth) * With probing pocket depth ≥ 5mm. * The age ranged between 45 and 60 years (To avoid the wide variation between individual cases in order to make the sample more homogeneous. Furthermore elderly patients above 60 years are usually not willing to have periodontal treatment). * Postmenopausal status for at least 1 year. * Presence of at least six teeth in the mouth.

Exclusion criteria

* Any systemic disease that affect the periodontium. * Women who take anti-inflammatory drugs, antibiotics or vitamins within the previous 3 month. * Women who use mouth washes regularly * Smoking * History of alcohol abuse * Participation in other clinical trials. * Obese women (Body mass index (BMI) ≥ 30).

Design outcomes

Primary

MeasureTime frameDescription
superoxide dismutase (SOD) activity in the gingival crevicular fluidup to 6 monthsSuperoxide dismutase activity in the gingival crevicular fluid was carried out at baseline, 3 and 6 months post treatment.

Secondary

MeasureTime frameDescription
Plaque Indexup to 6 monthsplaque index was recorded at baseline and at 3 and 6 months post treatment.
Gingival indexup to 6 monthsGingival index was recorded at baseline, 3, 6 months post treatment
Probing pocket depthup to 6 monthsProbing pocket depth in mm was recorded at baseline, 3, 6 months treatment
Clinical attachment levelup to 6 monthsClinical attachment level was recorded at baseline, 3 and 6 months post treatment

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026