COMPARISON OF THE TREATMENTOUTCOMES ON GUM DISEASE WITH THE USE OF PERIOGENâ?¢ AND BLOOD COMPONENT
Not Applicable
Completed
- Registration Number
- CTRI/2019/02/017391
- Lead Sponsor
- SAIRA SABA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 15
Inclusion Criteria
Inclusion Criteria
1.Systemically healthy subjects.
2.Patients 18-40 years of age.
3.Bilateral Millerâ??s class I and II gingival recession.
4.Patients with >=1mm of width of keratinized gingiva.
5.Patients with a thick gingival biotype.
6.Presence of good oral hygiene maintenance.
7.Non smokers
Exclusion Criteria
Exclusion Criteria:
1.Presence of dehiscence or fenestration.
2.Malposed teeth.
3.Root caries.
4.History of any periodontal surgery in same area in the past 6 months.
5.Pregnant or lactating women.
6.Patients on medications.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Prior to surgery an acrylic stent will be fabricated on the patients cast for standardization of the measurements to be assessed and following clinical parameters will be assessed in millimetres using UNC-15 Probe: <br/ ><br>1.Gingival recession depth. <br/ ><br>2.Gingival recession width. <br/ ><br>3.Probing depth. <br/ ><br>4.Clinical attachment level. <br/ ><br>5.Keratinized gingival width. <br/ ><br>Timepoint: AT BASELINE <br/ ><br>3 MONTHS POST SURGERY <br/ ><br>6 MONTHS POST SURGERY
- Secondary Outcome Measures
Name Time Method ILTimepoint: NIL <br/ ><br>