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The effect of synthetic material in gingival reconstructio

Not Applicable
Conditions
inadequate attached gingiva.
Disorder of gingiva and edentulous alveolar ridge, unspecified
Registration Number
IRCT2015051222249N1
Lead Sponsor
Vice chancellor for research, Qazvin university of medical sciences.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Patients referred to Qazvin faculty of dentistry in 2014, who need a gingival augmentation due to gingival diseases, trauma or anatomic variations. All the participants should: 1) Practice adequate oral hygiene procedures regularly. 2) Have at least one teeth with gingival height <= 1 mm in need of gingival augmentation. 3) Have a probing depth <=3 mm in aforesaid tooth. 4) Not have any systemic diseases. 5) Not be smoker. Exclusion criteria: Failure to attend the recall visits.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Attached gingiva width. Timepoint: baseline, 14 days post operation, 12 weeks post operation. Method of measurement: periodontal probe.
Secondary Outcome Measures
NameTimeMethod
Inflammation, periodontal pocket. Timepoint: baseline, 12 weeks post operation. Method of measurement: gingival index, probing depth.
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