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Comparing two treatment protocols in reducing Dentin hypersensitivity

Comparative Clinical Evaluation of two In-office Desensitizing agents in Reducing Dentin hypersensitivity- A Randomised Split Mouth Clinical Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077272
Enrollment
40
Registered
2024-11-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

None listed

Interventions

Intervention1: Resin based varnish: single coat applied on the buccal side of the cervical area of the teeth and light cured for 15 seconds Control Intervention1: sodium fluoride based Varnish: Applie

Sponsors

Dr Juttu Shirisha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients from 30 to 60 years of age with excellent systemic health conditions with history of dentin hypersensitivity with Preoperative Schiff scale of =1 and at least two or more lesions in two different quadrants of the mouth are included in this study

Exclusion criteria

Exclusion criteria: Patients who have used desensitizing toothpaste in the last 3 months, receiving periodontal therapy with cervical defects greater than 2mm horizontally, allergic to ingredients used in the study, chronic users of anti-inflammatory and analgesics, pregnant or nursing with uncontrolled systemic diseases, with fractured or cracked teeth are excluded from the study

Design outcomes

Primary

MeasureTime frame
Efficacy of varnishesTimepoint: baseline score, immediately, after 1 week

Secondary

MeasureTime frame
Efficacy of varnishesTimepoint: after 1 month

Countries

India

Contacts

Public ContactDr Umrana Faizuddin

Panineeya Institute of dental sciences and research centre

umranaafroz@rediffmail.com9949244418

Outcome results

None listed

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