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How periodontal treatment affects oral health-related quality of life in patients with chronic periodontitis

Phase 2
Recruiting
Conditions
Chronic periodontitis.
Chronic periodontitis
Registration Number
IRCT201709211081N8
Lead Sponsor
Private clinic, Dr. Golpar Radafshar, associate professor of periodontology, Guilan University of Me
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Inclusion criteria were a diagnosis of generalized moderate to severe chronic periodontitis and having at least 20 standing teeth. The exclusion criteria were a history of periodontal treatment 6 months prior to entry, taking any medication known to affect periodontal tissues, taking anti-depressant, anti-anxiety, anti-inflammatory, and immunosuppressive medications, uncontrolled diabetes, pregnancy or lactation, smoking, and needing antibiotic prophylaxis.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oral health-related quality of life. Timepoint: Baseline, after non-surgical, after surgical intervention. Method of measurement: Validated Iranian version of the Oral health impact profile questionnaire.
Secondary Outcome Measures
NameTimeMethod
Periodontal pocket depth. Timepoint: Baseline, after non-surgical, after surgical interventions. Method of measurement: Using a periodontal probe, distance from gingival margin to the base of the pocket is measured.;Clinical attachment level. Timepoint: Baseline, after non-surgical, after surgical interventions. Method of measurement: Using a periodontal probe, distance from a fix point to the base of pocket is measured.;Bleeding on probing. Timepoint: Baseline, after non-surgical, after surgical interventions. Method of measurement: Lenox & Kopczyk bleeding index.
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