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Treatment of exposed teeth with platelet concentrate or commercially available membrane.

Not Applicable
Conditions
Health Condition 1: K053- Chronic periodontitis
Registration Number
CTRI/2024/01/061419
Lead Sponsor
Institute of Dental Studies and Technologies
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Systematically healthy patients and patients having minimum two bilateral Cairo RT1/RT2 gingival recession defect.

Exclusion Criteria

Severe cervical abrasions or root caries requiring restoration

Aberrant frenal attachment

Malpositioned teeth

Smokers

Pregnant or lactating females

Patients having undergone any periodontal therapy in the last six months.

Antibiotic therapy in past 6 months.

Clotting and hematological disorders.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
With the use of stent- <br/ ><br>•Probing Pocket Depth (PPD): [(FRP-BOP) – (FRP-GM)] <br/ ><br>•Clinical Attachment Level (CAL): [(FRP-BOP) – (FRP-CEJ)] <br/ ><br>•Gingival Recession (GR): [(FRP-GM) – (FRP-CEJ)] <br/ ><br>•Width of Keratinized Gingiva (KT): [(FRP-MGJ) – (FRP-GM)] <br/ ><br>Without the use of stent- <br/ ><br>1.Width of Recession (At CEJ) <br/ ><br>2.Thickness of Gingiva (Mid buccal of the attached gingiva irt the selected site using an endodontic file with stopper and a digital vernier caliper.) <br/ ><br> <br/ ><br>Timepoint: 3 MONTHS AND 6 MONTHS
Secondary Outcome Measures
NameTimeMethod
Root Coverage Esthetic Score (RES) and percentage of Root Coverage.Timepoint: 6 MONTHS
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