Comparing dental sensitivity after restoring teeth with two novel dental materials

Comparative Evaluation of Post Operative Sensitivity in Non Carious Cervical Lesions restored with Giomer and Nanoceramic composite Resin- An In Vivo Study

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/06/019949

Enrollment

120

Registered

2019-06-28

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Giomer: Giomer using self etch adhesive with self etch mode. Primer will be applied to the cavity surface for 10 seconds and cured for 5 seconds. Giomer will be applied into the cavity

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with at least 24 natural teeth 2. Patients having at least 2 contralateral teeth with non carious cervical lesions indicated for restoration 3. Depth of lesions being 4. Patients willing to participate in study for 6 months 5. Patients with good oral hygiene

Exclusion criteria

Exclusion criteria: 1. Carious teeth 2. Patients with history of spontaneous pain / sinus tract 3. Patients with class V lesions extending below cemento-enamel junction 4. Patients having parafunctional habits 5. Patients using any desensitizing toothpaste or mouthwash 6. Patients with active periodontal disease or those who have undergone periodontal surgery during last 6 months 7. Patient allergic to resin based materials 8. Asthmatic patients 9. Patients taking regular NSAIDS, psychotropic drugs or medications for other systemic diseases 10. Pregnant or lactating mothers

Design outcomes

Primary

Measure	Time frame
Patients will be evaluated for presence or absence of post operative sensitivity after the defined recall period.Timepoint: 24 hours, 1 month, 3 months, 6 months	—

Secondary

Measure	Time frame
Intensity of post operative sensitivity will serve as the secondary outcome for the study. Report from patient regarding dentinal hypersensitivity, air blast test and cold water will be recorded and scored according to Visual Analogue Scale(VAS scale).Timepoint: 24 hours, 1 month, 3 months, 6 months	—

Countries

India

Contacts

Public ContactDR POONAM BOGRA

J.N KAPOOR D.A.V DENTAL COLLEGE

poonambogra@yahoo.in9050462962

Outcome results