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A clinical trial to evaluate the use of adhesives in class V dental restorations done using a new alkasite dental cement - Cention N.

A RANDOMIZED DOUBLE-BLIND ACTIVE CONTROLLED CLINICAL TRIAL TO COMPARE THE EFFECT OF USE OF ADHESIVES ON THE CLINICAL OUTCOME IN CLASS V RESTORATIONS USING CENTION N , A DIRECT FILLING ALKASITE MATERIAL & PACKABLE GLASS IONOMER CEMENT IN CHILDREN AND YOUNG ADULTS

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/09/015814
Enrollment
32
Registered
2018-09-24
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

Health Condition 1: K026- Dental caries on smooth surface Health Condition 2: K029- Dental caries, unspecified

Interventions

Intervention1: A NEW ALKASITE DENTAL CEMENT: A NEW ALKASITE DENTAL CEMENT BY TRADE NAME OF CENTION-N. Amount : that will be required to fill class V cavity (dimensions :a box-shaped class V cavity wi

Sponsors

DR HIMANSHU AERAN
Lead Sponsor
DR ADITI SINGH
Collaborator
DR PREETI DHAWAN
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1) 5-14 year old individual (both males and females) of districts of Uttarakhand. 2) Participants who have bilateral class V cavities in anterior teeth/premolars in primary/mixed /permanent dentition. 3) Individuals with a no systemic illness or psychological disorder of any kind 4) Individuals who do not have any removable appliance where the teeth in concern act as abutment tooth. 5) Individuals who do not have any malocclusion or TMJ related disorder. 6) The teeth in question should be periodontally sound and without any pulpal pathology. 7) Individuals who fulfill the research criteria and are ready to give the consent to participate in the study are considered for the study.

Exclusion criteria

Exclusion criteria: 1) Children below the age of 5years and above the age of 14 years. 2) Participants who refuse to participate in the study. 3) Subjects who are uncooperative for clinical examination during the study. 4) Subjects with any type of severe systemic disease or hypoplastic teeth or with persistent faulty oral habits. 5) Individuals with periodontally compromised teeth or pulpally involved anterior teeth / premolars. 6) Individuals with missing posterior teeth or malocclusion or TMJ disorder. 7) Individuals who canâ??t comply for a follow up of upto 2 years.

Design outcomes

Primary

MeasureTime frame
dentinal hypersensitivity shall be checked using Visual Analog Scale with the help of air blast using a three way syringe and tactile sensitivity shall be checked using 17/23 explorer repeated three times before recording.Timepoint: 0,6months,12months,18months,24 months—

Secondary

MeasureTime frame
retention, marginal adaptation, anatomic form, surface texture and secondary cariesTimepoint: 0,6months,12months,18months,24 months—

Countries

India

Contacts

Public ContactDR ADITI SINGH

SEEMA DENTAL COLLEGE & HOSPITAL

preetidhawan10@gmail.com08937815218

Outcome results

None listed

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