To check the efficiency of a new tissue displacing system- A Clinical Study

COMPARATIVE EVALUATION OF THE EFFICACY OF A NEW TISSUE DISPLACING IMPRESSION SYSTEM WITH CONVENTIONALLY USED GINGIVAL DISPLACEMENT MATERIALS AND TECHNIQUES ON GINGIVAL DISPLACEMENT - AN IN VIVO STUDY

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/08/027337

Enrollment

Registered

2020-08-24

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: GINGIVAL DISPLACEMENT: DIFFERENT GINGIVAL RETRACTION AGENTS WILL BE USED AND EFECT ON TISSUE DISPLACEMENT WILL BE STUDIED after 10 minutes of displacement Control Intervention1: GINGIVA

Eligibility

Inclusion criteria

Inclusion criteria: a) Individuals between the age group of 20-25 years. b) Good gingival health c) Thick gingival biotype

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
To evaluate the clinical efficacy of Retraction cord impregnated with astringent solution, Expasyl retraction paste and NoCord VPS Impression system to produce gingival displacement.Timepoint: the retraction will be assessed 5 - 10 minutes of retraction	—

Secondary

Measure	Time frame
To compare thedimensional accuracy of casts produced after tissue displacement with Retraction cord impregnated with astringent solution, Expasyl retraction paste and NoCord VPS Impression system.Timepoint: after 24 hrs of cast pouring	—

Countries

India

Contacts

Public ContactDr VIJETA GAJBHIYE

VSPM dental college and research centre

viju07gajbhiye@gmail.com9890324934

Outcome results