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Comparison of effect of two different blood products for the treatment of receeding gums- A controlled randomized clinical study

Phase 4
Conditions
Health Condition 1: K060- Gingival recession
Registration Number
CTRI/2023/06/053877
Lead Sponsor
Dr. Richa Saroj
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Participants between 18 and 50 years of age

2.Cairo Class I or II gingival recession defects measuring >= 2mm.

3.Vital teeth, free of faulty restorations.

4.Patients who gave informed consent for the study.

Exclusion Criteria

1.History of smoking or tobacco consumption

2.Pregnant or lactating women

3.Patient with active periodontal infection.

4.Patients with systemic condition that contraindicate surgery.

5.Patients with removable or fixed dentures in the area of interest.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Width of keratinized Tissue <br/ ><br>2. Recession Height <br/ ><br>3. Recession WidthTimepoint: Baseline - on the day of surgery & at 3 months
Secondary Outcome Measures
NameTimeMethod
1. Percentage Root Coverage <br/ ><br>2. Thickness of Attached GingivaTimepoint: Baseline- on the day of surgery & at 3 months
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