To check the efficiency of a new tissue displacing system- A Clinical Study
Phase 1
- Registration Number
- CTRI/2020/08/027337
- Lead Sponsor
- Dr Vijeta Gajbhiye
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
a) Individuals between the age group of 20-25 years.
b) Good gingival health
c) Thick gingival biotype
Exclusion Criteria
a) Thin gingival biotype
b) Malocclusion
c) Crowding , Rotation, Diastema
d) Regressive alterations of the teeth
e) Carious teeth
f) Restored anterior teeth
g) Systemic diseases
h) Known allergy to material used
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the clinical efficacy of Retraction cord impregnated with astringent <br/ ><br>solution, Expasyl retraction paste and NoCord VPS Impression system to produce <br/ ><br>gingival displacement.Timepoint: the retraction will be assessed 5 - 10 minutes of retraction
- Secondary Outcome Measures
Name Time Method To compare thedimensional accuracy of casts produced after tissue displacement with Retraction cord impregnated <br/ ><br>with astringent solution, Expasyl retraction paste and NoCord VPS Impression <br/ ><br>system.Timepoint: after 24 hrs of cast pouring