MedPath

Effect of phenytoin mucoadhesive paste 1% on periodontal parameters

Phase 2
Conditions
Chronic periodontitis.
Chronic periodontitis
Registration Number
IRCT2014081718834N1
Lead Sponsor
Vice chancellor for research of Shahid Sadoughi Dental Faculty
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Inclusion criteria were considered as follows: having ability to read and write, no systemic diseases such as diabetes or heart disease, not taking medications affecting periodontium (anti- hypertensives, immune suppressants and anticonvulsants), not being pregnant, no smoking, no traumatic occlusion, no history of antibiotic therapy within the last three months, having at least two similar teeth on each sextants without any decays or restorations and filling informed consent form. In addition we consulted with internist about any drug interactions to phenytoin in patients of our study. The exclusion criteria were considered as follows: 1) inappropriate control plaque during the study. 2) irregular use of pastes on the basis of given instructions 3) not taking part in following up appointments.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pocket depth. Timepoint: 4 weeeks. Method of measurement: milimeters by Williams’s periodontal probe.;Bleeding on probing. Timepoint: 4 weeks. Method of measurement: percentage.;Modified gingival index. Timepoint: 4 weeks. Method of measurement: grading by observation.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath