Evaluation of Nucleotide-Binding Oligomerization Domain-Containing Protein (NOD) 1 and NOD 2

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMedipol University

About this trial

The host immune response to microorganisms is primarily recognized by pattern recognition receptors (PRRs), including toll-like receptors and nucleotide-binding oligomeric domain (NOD) receptors (NLRs). The aim of this study was to examine the relationship between periodontal disease and NOD in serum and saliva samples.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

systemically healthy

clinical diagnosis of periodontal health

clinical diagnosis of periodontitis

clinical diagnosis of gingivitis

Disqualifiers

• history of regular use of systemic antibiotics anti-inflammatory, or antioxidant drugs (previous 3 months)

nonsurgical periodontal treatment (previous 6 months)

surgical periodontal treatment (previous 12 months)

presence of<10 teeth

Trial design

Design model

Single group

Treatments tested in this trial

  • Saliva and Serum sampling

    Other intervention

    Saliva were collected to analyze the selected markers as unstimulated samples during the early hours of the day. The saliva was centrifuged and then transferred into Eppendorf tubes. Venous puncture was performed after saliva collection and 5 mL of blood samples were collected by qualified staff from each participant.Saliva and serum were then stored at -80 °C until analysis.

  • Saliva and Serum sampling

    Other intervention

    ELISA method will be used to measure IL-10 and IL-6 values in collected saliva and serum samples. For ELISA analysis, a commercial kit (Sunred Bio, Shanghai, China) pre-coated with human selected antibodies will be used.

Treatment groups

75 Participants
are divided into 2 treatment groups
Group A: Active ComparatorActive comparator 1 intervention
Group B: ExperimentalExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pocket probing depth

Measurement of the depth of a sulcus or periodontal pocket determined by measuring distance from a gingival margin to the base of the sulcus or pocket with a calibrated periodontal probe.

Time frame
6 months
2

Clinical attachment level

Clinical attachment level (or loss, CAL) is a more accurate indicator of the periodontal support around a tooth than probing depth alone. CAL is measured from a fixed point on the tooth that does not change, the CEJ. To calculate CAL, two measurements are needed: distance from the gingival margin to the CEJ and probing depth. In recession: probing depth (+) gingival margin to the CEJ (add). In tissue overgrowth: probing depth (-) gingival margin to the CEJ (subtract)

Time frame
6 months
3

Bleeding on probing

Referring to bleeding that is induced by gentle manipulation of the tissue at the depth of the gingival sulcus, or interface between the gingiva and a tooth.

Time frame
6 months

Secondary outcomes

1

Saliva and serum samples processing and analyses

Saliva and serum samples obtained for each patient were used for cytokine analysis. Prepared samples were analyzed for NOD1, NOD2, IL-10 and IL-6 using commercial ELISA kits

Time frame
1 month

Other outcomes

Sponsors and contacts

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