Skip to content

Comparison of two flowable composite in non-carious cavity of the teeth: A Randomised clinial trial.

Clinical performance of two flowable resin based composite in non-carious cervical lesions of the teeth: A Split mouth, Double blinded Randomised clinical trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084414
Enrollment
30
Registered
2025-04-08
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: K031- Abrasion of teeth

Interventions

Intervention1: Placement of two flowable resin based composite with and without retentive slots in non-carious cervical lesions of the teeth.: Evaluation of two flowable resin based composite in non-c

Sponsors

JSS AHER grants
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Must be above 18 years. 2. Must be given written consent to participate in the trail. 3. Must be in good general health. 4. Must be available for the required post-operative follow-up visits. 5. Must have a minimum of 4 cervical lesions in need of restoration. 6. Cervical lesions must provide for a minimum of 1mm thickness of restorative material while maintaining natural tooth contour. 7. Participants with the score of 3 of Tooth Wear Index by Smith and Knight will be selected

Exclusion criteria

Exclusion criteria: 1. Systemic or local disorders that contraindicate the dental procedures. 2. Evidence of xerostomia, severe bruxing or clenching or in need of TMJ related therapy. 3. Pregnant (self-reported) and lactating women. 4. Known allergy to dental materials. 5. Any oral soft tissue lesions 6. Are unwilling or unable to have dental radiographs or photographs taken of their dentition or soft tissues 7. Condition affecting salivary flow (e.g., salivary gland disorder, Sjögren’s Syndrome) 8. Any other condition which in the view of the investigator may affect the ability of a subject to complete the study 9. Teeth with periapical pathology or exhibiting symptoms of pulpal pathology and teeth that have been pulp capped 10. Non-vital and root canal treated teeth. 11. Teeth with near pulpal exposures on pre-operative radiographs 12. Hypersensitive teeth 13. Teeth with a periodontal pocket of more than 4mm with bleeding on probing 14. Teeth that are used as abutments for any prosthesis.

Design outcomes

Primary

MeasureTime frame
To compare and evaluate the treatment outcome between flowable Giomer and Nanohybrid composite resin using modified Hickel criteria.Timepoint: 18 months

Secondary

MeasureTime frame
To compare and evaluate the outcome between flowable Giomer (with retentive slot), (without retentive slot) and Nanohybrid composite resin (with retentive slot), (without retentive slot)Timepoint: 18 months

Countries

India

Contacts

Public ContactDr Annapoorna BM

JSS Dental College and Hospital, Mysuru

dr.annapoornabm@jssuni.edu.in9611091429

Outcome results

None listed

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