Scaling effect on 2 salivary factors in patients with gingival inflammatio

Not Applicable

• Conditions: Chronic Periodontitis.; Chronic periodontitis

• Registration Number: IRCT2016053025649N5
• Lead Sponsor: Kermanshah Uninersity of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

good general health with no history of any systemic disease, no history of antibiotic therapy during 2 months before the study begins; no history of NSAID therapy.
Exclusion criteria: smoking or alcohol abuse; patients with mucousal inflammatory lesions such as lichen planus or salivary glands disorders; pregnant or lactating females.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
IL-6. Timepoint: 1 month after scaling. Method of measurement: Mesured by specialized ELISA KIT.;IL-17. Timepoint: 1 month after scaling. Method of measurement: Mesured by specialized ELISA KIT.;Pocket depth. Timepoint: screening day , 1 month after scaling. Method of measurement: Mesuring the distance of pocket base to the gingival margin with periodontal probe.;Clinical attachment loss. Timepoint: screening day , 1 month after scaling. Method of measurement: Mesuring the distance of pocket base to the CEJ. Any changes in this normal amount is defined as clinical attachment loss.;Plaque index. Timepoint: screening day , 1 month after scaling. Method of measurement: colored surfaces of tooth by disclosing agent.;Bleeding on probing. Timepoint: screening day , 1 month after scaling. Method of measurement: Observe bleeding after probing.