Evaluation of the influence of various gingival biotypes on the healing capacity of marginal gum tissue in gums with shallow recession defects following non surgical periodontal treatment- A Prospective Study

Not Applicable

• Conditions: Health Condition 1: K055- Other periodontal diseases

• Registration Number: CTRI/2020/08/026986
• Lead Sponsor: Dr Shabistan N Farooqi

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1)Male and female participants

2)Age between 18-40 years

3)Participants with healthy periodontium and very good oral hygiene with full-mouth

plaque score (FMPS) <20% , full-mouth bleeding score (FMBS) <=20 %.

4) Millerâ??s Class 1 buccal gingival recession with recession depth <= 2mm on teeth

incisors ,canines or premolars with an identifiable cemento-enamel junction (CEJ).

5) Gingival recession associated with tooth brushing trauma or plaque-induced

inflammation.

6) Vital teeth.

7) Participants with good physical health .

Exclusion Criteria

1)Pregnant women and lactating mothers.

2) Participants who have undergone surgical or non-surgical periodontal therapy.

3) Participants taking medication associated with gingival enlargement (i.e cyclosporin

A, phenytoin or calcium channel blocker)

4) Any caries ,cervical abrasion on CEJ of the tooth, restorations on cervical area.

5) Smokers

6) Participants with systemic diseases or medical history

7) Participants with indications for surgical coverage .

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To assess the influence of Gingival Biotypes on the Restorative Capacity of Marginal Gingiva <br/ ><br>in Shallow Gingival Recession over a period of 3 months following non-surgical periodontal <br/ ><br>therapy .Timepoint: baseline,at every two weeks for first month ,once every month for next 2 months

Secondary Outcome Measures

Name	Time	Method
To measure the probing depth and clinical attachment loss of selected tooth following <br/ ><br>non-surgical periodontal therapy of scaling, root planning and polishing at baseline and 3 <br/ ><br>months after non-surgical periodontal therapyTimepoint: baseline,at every two weeks for first month ,once every month for next 2 months