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Clinical effects of subantimicrobial dose doxycycline

Not Applicable
Conditions
Clinical effects of subantimicrobial dose doxycycline.
Other specified disorders of teeth and supporting structures
Registration Number
IRCT201205058205N2
Lead Sponsor
Vice chancellor for research, Shahid Sadoghi University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
44
Inclusion Criteria

Inclusion criterion: having at leat 14 untreated teeth with mild periodontitis in two quadrantsthat need comprehensive treatment.
Exclusion criteria were: pregnant women; patients with a history of tetracycline sensitivity; any sytemic infection requiring antibiotic prophylaxy for dental procedures; history of intake of tetracycline during the 3 last months; history of periodontal therapy (scaling and root planing or periodontal surgery) during the last 3 months.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
PPD: The distance between the gingival margin and depth of sulcus. Timepoint: Before treatment, 3 months after treatment. Method of measurement: Periodontal probe, mm.
Secondary Outcome Measures
NameTimeMethod
BOP: bleeding on probing. Timepoint: Before treatment, 3 months after treatment. Method of measurement: Periodontal probe,mm.;CAL: The distance between cementoenamel junction (CEJ) and the bottom of pocket. Timepoint: Before treatment, 3 months after treatment. Method of measurement: Periodontal probe,mm.;MGI: a gingival index for evaluation of gingival health. Timepoint: Before treatment, 3 months after treatment. Method of measurement: Periodontal probe,mm.
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