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A clinical trial to study the effect of surface treatment of non carious cervical lesion with different chemicals on clinical performance of composite resin restoration.

Evaluation of clinical performance of nano filled composite restoration placed for treating non carious cervical lesion after application of three different MMP inhibitors - Randomized control trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/051120
Enrollment
40
Registered
2023-03-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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: Chlorhexidine: 2% chlorhexidine digluconate will be applied once only after the preparation of NCCL followed by restoration with nanofilled composite which will be evaluated at 6 months

Sponsors

Dr Shrutika Jadhav
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Vital teeth Lesion depth 1-2mm Fair oral hygiene Esthetic purpose Cervical lesion beyond (DEJ)

Exclusion criteria

Exclusion criteria: Poor Oral Hygiene Heavy Bruxism Pathological pulpal diagnosis with pain Carious Lesion Fractured Teeth Lack of written Informed Consent to Participate Underage Patients Pregnant or nursing women Infectious Diseases Mucosal diseases with unclear diagnosis Non vital pulp Severe periodontal diseases

Design outcomes

Primary

MeasureTime frame
Clinical performance of nanofilled composite restoration in intervention groups (ie MMP inhibitor) will be assessed and compared to that of control group for its superiority inferiority or no effect according to USPHS criteriaTimepoint: 2 weeks (baseline)3 months 6 months 12 months

Secondary

MeasureTime frame
Clinical performance of nanaofilled composite restoration in intervention groups (ie MMP inhibitor groups) will be compared amongst them self (without comparing it to control group) for superiority inferiority or no effect according to USPSHS criteriaTimepoint: 2 weeks(baseline) 3 months 6 months 12 months

Countries

India

Contacts

Public ContactDr Shrutika Jadhav

Dr Hedgewar Smruti Rugna Seva Mandals Dental College and Hospital

rajiv.khode@gmail.com918208899410

Outcome results

None listed

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