Skip to content

Effect Of Non-Surgical Periodontal Treatment On Lipoxin a4 Levels

Effect Of Non-Surgical Periodontal Treatment On Endogenous Anti-Inflammatory Lipid Mediators In Patients With Chronic Periodontitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04053660
Enrollment
20
Registered
2019-08-12
Start date
2017-10-01
Completion date
2018-12-31
Last updated
2019-08-12

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

Conditions

Periodontitis

Keywords

Gingival Crevicular Fluid, Lipid Mediator, Periodontal Treatment

Brief summary

The aim of this study was to evaluate the levels of lipoxin A4 (LXA4), prostaglandin E2 (PGE2) and leukotriene B4 (LTB4) in gingival crevicular fluid (GCF) and saliva in individuals with periodontal healthy and chronic periodontitis. In addition, the investigators evaluated the levels of these mediators after non-surgical periodontal treatment in patients with chronic periodontitis. A total of 20 subjects, 10 patients with chronic periodontitis (CP) and 10 periodontally healthy individuals were included in the study. Clinical parameters including plaque index (PI), gingival index (GI), probing depth (PD) and clinical attachment levels (CAL) were recorded. GCF and saliva samples were obtained at the beginning of the study from all individuals. GCF and saliva samples were re-collected from patients with CP at 1 month after non surgical periodontal therapy.

Interventions

PROCEDURENon-surgical periodontal treatment

Mechanical non-surgical treatment were performed

Sponsors

Ordu University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Have at least 20 natural teeth, excluding third molars. * Chronic periodontitis patients had at least two non-adjacent sites per quadrant with probing depth (PD) ≥ 5 mm and clinical attachment level (CAL) ≥ 5 mm with gingival inflammation, and alveolar bone loss affecting \>30% of the teeth, as detected on clinical and radiographical examinations. * Periodontally healthy control group had no sign of gingival inflammation, no PD \> 3mm and no evidence of attachment or bone loss.

Exclusion criteria

* History of systemic disease. * Regular use of any drugs which can effect the immune system or inflammatory response in the 6 months preceding the start of the study. * Periodontal treatment during last 6 months that could affect periodontal status. * Smoking. * History of radiotherapy or chemotherapy. * Ongoing orthodontic treatment. * Aggressive periodontitis. * Current pregnancy, lactation or menopause.

Design outcomes

Primary

MeasureTime frameDescription
Lipoxin A4 levels1st monthchange of gingival crevicular fluid and salivary Lipoxin A4 levels from baseline at 1st month

Secondary

MeasureTime frameDescription
Prostaglandin E2 levels1st monthchange of gingival crevicular fluid and salivary Prostaglandin E2 levels from baseline at 1st month
Leukotriene B41st monthchange of gingival crevicular fluid and salivary Leukotriene B4 levels from baseline at 1st month

Countries

Turkey (Türkiye)

Outcome results

None listed

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