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A Comparative Study of Evaluation of restoring caries with 2 surfaces using Convential Composite material with Newly Introduced Composite material with glass fibres using clear matrix.

Comparative Evaluation of Conventional Composite Restoration Technique with New Injectable Fibre Reinforced Composite using Clear Silicone Putty Index Technique in Class 1 Compound Carious Lesions-A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/09/027860
Enrollment
20
Registered
2020-09-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: K029- Dental caries, unspecified

Interventions

Intervention1: (a)GC Ever X Flow (b)G-aenial Universal Injectable (c)EXACLEAR: Ever X Flow is a short-fibre reinforced flowable composite for dentine replacement. G-aenial Universal Injectable is a u

Sponsors

Dr Supreet Kaur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between 18 ââ?¬â?? 60 years of age with moderately deep Class I Compound lesions of molars with undermined lesions will be included in the study. 2. Teeth with radiographic findings revealing radiolucency in coronal dentin will be included. 3. Teeth with intact occlusal anatomy will be included. 4. Teeth with secondary decay or fracture of old amalgam and composite fillings will be included. 5. Teeth with opposite and adjacent tooth in contact will be included. 6. A written informed consent will be taken from all the patients and only those patients ready to sign the consent form will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patients with poor oral hygiene will be excluded from the study. 2. Patients with severe or chronic apical periodontitis and heavy bruxism will be excluded. 3. Patients with malocclusion rotated teeth or attrited teeth will be excluded. 4. Teeth with pulpal and/ or periapical pathology will be excluded. 5. Teeth with developmental anomaly or pathology or congenital defects will be excluded. 6. Teeth which have to be used as an abutment will be excluded. 7. Pregnant and lactating women will be excluded

Design outcomes

Primary

MeasureTime frame
To detect marginal discoloration, marginal adaptation, secondary caries, anatomic form, post-operative sensitivity,color match, and retention.Timepoint: 3 months and 6 months

Secondary

MeasureTime frame
To detect time taken for procedureTimepoint: 3 months and 6 months

Countries

India

Contacts

Public ContactSupreet Kaur

Sumandeep Vidyapeeth

drkishankv@yahoo.co.in8141787335

Outcome results

None listed

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