cervical fillings

Evaluation of new alkasite based restorative material for restoring non carious cervical lesions- Randomized controlled clinical trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/08/015252

Enrollment

Registered

2018-08-09

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

Health Condition 1: R948- Abnormal results of function studies of other organs and systems Health Condition 2: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention1: Cention N: alkasite cement Control Intervention1: Resin modified glass ionomer cement: Glass ionomer cement

Eligibility

Inclusion criteria

Inclusion criteria: vital teeth good oral hygiene absence of periodontal disease normal occlusion with interproximal contact

Exclusion criteria

Exclusion criteria: non-vital teeth teeth with parafunctional tooth wear cervical caries poor oral hygiene discoloations periodontitis mobile teeth subgingival lesions

Design outcomes

Primary

Measure	Time frame
Longitivity of cervical restorationsTimepoint: 1 month 6 months 1 year	—

Secondary

Measure	Time frame
Retention and Marginal integrity of cervical restorationsTimepoint: 1 year	—

Countries

India

Contacts

Public ContactVasudev Ballal

Professor

drballal@yahoo.com09880626167

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026