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Clinical Durability and Longevity of Cervical Composite restorations - A One Year follow-up Clinical study

Evaluation of Longevity of Cervical restorations using Gingival Composite: A Randomized Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/10/046298
Enrollment
20
Registered
2022-10-10
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: K031- Abrasion of teeth

Interventions

Intervention1: Gingival Composite: Restoration of teeth with Cervical Abrasion using Gingival Composite and the restorations will be evaluated using FDI criteria at 1,3,6 and 12 months Control Interve

Sponsors

YASMEEN MOHAMMED AZEEM
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Volunteers with the presence of at least two non-carious cervical lesions, permanent dentition with age group of 18 ââ?¬â?? 65years, cervical margin in dentin, vital pulp with absence of symptoms of pulpitis such as spontaneous pain or sensitivity to pressure and with good oral hygiene.

Exclusion criteria

Exclusion criteria: Volunteers with severe periodontal disease, severe systemic diseases, allergy to any material used, very poor oral hygiene, pregnant or breast feeding, exposure to overload due to crowding of teeth and cervical carious lesions.

Design outcomes

Primary

MeasureTime frame
Primary outcome: Evaluation of longevity of restoration using FDI criteria Timepoint: Baseline, 3months, 6 months and 12 months

Secondary

MeasureTime frame
Secondary outcome: Quality of life using OHIP 14 criteriaTimepoint: Baseline, 3months, 6 months and 12 months

Countries

India

Contacts

Public ContactYasmeen Mohammed Azeem

Narayana Dental College And Hospital, Nellore

govulakiranmayi24@gmail.com9440932608

Outcome results

None listed

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