MedPath

A study to compare two tooth coloured filling materials.

Phase 3
Not yet recruiting
Conditions
non-carious cervical lesions in maxillary teeth
Registration Number
CTRI/2021/08/035461
Lead Sponsor
CHRISTIAN DENTAL COLLEGE
Brief Summary

It is a randomized interventional clinical study conducted on 30 periodontally healthy patients with split-mouth approach comparing the periodontal health and clinical performance of Resin modified glass ionomer with Activa bioactive restorative material in non-carious cervical lesions and the patients will be followed up for 18 months.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

•Bilateral non carious cervical lesions in Maxillary arch •Age group- 29-65 years •Etiology: Abrasive toothpaste and faulty brushing technique •Periodontally healthy teeth.

Exclusion Criteria

•Patient with systemic disorder or under antibiotic or anti-inflammatory therapy •Traumatic occlusion •Parafunctional habits or anomalies like high frenal attachment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Periodontal health of non–carious cervical lesions in teeth restored with RMGI(Light cured GIC) and a bioactive restorative material(Activa Bioactive) upto 18 months.3months | 6months | 12months | 18months
2.Marginal adaptation of the restorations upto 18 months3months | 6months | 12months | 18months
Secondary Outcome Measures
NameTimeMethod
Post operative sensitivity, surface texture, contour, marginal discolouration, recurrent caries in restored teeth.3months

Trial Locations

Locations (1)

CHRISTIAN DENTAL COLLEGE

🇮🇳

Ludhiana, PUNJAB, India

CHRISTIAN DENTAL COLLEGE
🇮🇳Ludhiana, PUNJAB, India
GAURI MALIK
Principal investigator
9217133366
gaurimlk@gmail.com

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