comparison between resin modified glass ionomer cement and universal injectable composite in non carious cervical lesions

Comparative clinical evaluation of resin modified glass ionomer cement and universal injectable composite in non-carious cervical lesions: a prospective randomised clinical trial - NIL

Status

Active, not recruiting

Phases

Phase 1Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/08/092803

Enrollment

Registered

2025-08-11

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

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

Conditions

None listed

Interventions

Intervention1: Universal injectable composite: Universal injectable composite material is the new material came into the market. Has excellent esthetics, good flexural strength and properties to be us

Eligibility

Inclusion criteria

Inclusion criteria: Co-operative healthy subjects willing to participate in the study and sign the consent form. Subjects having a minimum of 2 such noncarious cervical lesions in their mouth. Subjects having noncarious cervical lesions involving enamel and dentin. Subjects having good oral hygiene. Subjects aged 18 years and above of either gender. Subjects should have at least 20 permanent teeth.

Exclusion criteria

Exclusion criteria: Subjects unwilling to sign the consent form. Previously restored or fractured teeth. Medically compromised, mentally challenged adults. History of existing tooth sensitivity. Known allergy to resin based materials. Bruxism. Pregnancy or breast feeding subject. Subjects with restricted mouth opening. Chronic use of anti-inflammatory, analgesics and psychotropic drugs.

Design outcomes

Primary

Measure	Time frame
Clinical performanceTimepoint: at baseline	—

Secondary

Measure	Time frame
NILTimepoint: NIL	—

Countries

India

Contacts

Public ContactDr Rahul Rao

Bharti vidyapeeth dental college and hospital, Navi mumbai

drrahulrao25@gmail.com09820094178

Outcome results