Post-operative sensitivity in non carious cervical lesions using Universal adhesives

Evaluation of post-operative sensitivity in non carious cervical lesions using two Universal adhesives in different adhesive strategies - A Double-blinded Randomized controlled clinical trial.

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/11/038198

Enrollment

Registered

2021-11-23

Start date

Unknown

Completion date

Unknown

Last updated

2022-02-21

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 Health Condition 2: K031- Abrasion of teeth

Interventions

Intervention1: Universal adhesives in Self-etch adhesive strategy: Use of self-etch adhesive strategy using two Universal ahesives namely Singlebond Universal (3M ESPE) and Prime and Bond Universal (D

Eligibility

Inclusion criteria

Inclusion criteria: patients 30-50 years of age atleast 2 NCCLs in each quadrant depth of the lesion 1-3mm, presence of antagonist teeth.

Exclusion criteria

Exclusion criteria: poor gingival and periodontal health; uncontrolled rampant caries; bruxism; patients with systemic diseases.

Design outcomes

Primary

Measure	Time frame
Reduced VAS score for assessment of postoperative sensitivity at 24 hrs, 1week, 2weeks, 4 weeks.Timepoint: 24 hrs, 1week, 2weeks, 4 weeks.	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactDr Krisha Doshi

Saveetha Dental COllege and Hospitals, Chennai

nivedhitha@saveetha.com9840912367

Outcome results

None listed

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