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comparative evaluation of post operative sensitivity using three different restorative materials in non-carious cervical lesions.

Comparative evaluation of the postoperative sensitivity using resin modified glass ionomer cement, zirconomer and flowable composites in noncarious cervical lesions.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/040682
Enrollment
30
Registered
2022-02-28
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: K119- Disease of salivary gland, unspecified

Interventions

Intervention1: ZIRCONOMER, FLOWABLE COMPOSITE: ZIRCONOMER, FLOWABLE COMPOSITE Control Intervention1: RESIN MODIFIED GIC: RESIN MODIFIED GIC

Sponsors

Sharad Pawar Dental College Sawangi Meghe Wardha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient selection- 1 30 consented patients between 25ââ?¬â??40 years of age 2 Non-smoker 3 Good general health of the patient without relevant disease 4 Good oral hygiene 5 Patients having good periodontal health 6 Patients suffering from tooth sensitivity 7 Who are concerned about esthetics were included in the study. 8 low caries index Teeth selection- 1 Probing depth (PD) 2 NCCL depth 1-2 mm 3 Presence of >1 mm highly keratinized tissue apical to the root exposure, and presence of >0.8 mm-thick gingival tissue. 4 Wedge or saucer-shaped lesions 5 Preserved vitality of teeth 6 Absence of periodontitis, periradicular lesions, traumatic occlusion, bruxism, and wear facets. 7 Possibility to get proper isolation by rubber dam.

Exclusion criteria

Exclusion criteria: Exclusion criteria � Medically compromised patients, patients with severe periodontitis, high caries risk, heavy bruxism, xerostomia, fractured or cracked tooth, pregnant or breastfeeding mothers were excluded. � Patients with mobile or fixed prosthetic restorations in the immediate environment of the tooth restorations. � Patients with any systemic disorder, and a positive history of antibiotic and analgesic use within the week before the treatment. � Teeth having cervical caries, fractures, pulpal involvement periapical pathology, mobility, and restoration involving the buccal surfaces were excluded from the study.

Design outcomes

Primary

MeasureTime frame
Post operative sensitivity in noncarious cervical lesions.Timepoint: post operative sensitivity will be assessed at baseline, 3 days, 7 days, 21 days.—

Secondary

MeasureTime frame
Not applicableTimepoint: Not applicable—

Countries

India

Contacts

Public ContactDr Radhika Gupta

Datta meghe institute of medical sciences, sawangi, wardha 442001

adityasinghpatel@gmail.com8767319159

Outcome results

None listed

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