Assessment of benefits of Two Desensitizing Toothpastes (Toothmin and Perfora) for Tooth Sensitivity and evaluation of its effect in Saliva composition

The Effect of commercially Available Toothpast (Toothmin & Perfora) on Salivary Biomarkers and Clinical Parameters in Patients with Dentinal Hypersensitivity: A Randomized Controlled Trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103126

Enrollment

Registered

2026-02-05

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

None listed

Interventions

Intervention1: performa &Toothmin toothpaste: the study participants will be asked to use this toothpaste twice daily using provided tooth brush. They will be asked to use for 6 weeks Control Interven

Eligibility

Inclusion criteria

Inclusion criteria: systemically helathy male and female pt woth age range of 25-65yrs willing to participate in the study patients having positive response for at least two teeth on clinical examination for dentinal hypersensitivity

Exclusion criteria

Exclusion criteria: pregnant and lactating woman patient who is already on treatment for dentinal hypersensitivity pateint with allergy patent who are receiving treatment for GERD patients with systemic illness or any other oral pathology

Design outcomes

Primary

Measure	Time frame
reduction in dentinal hypersensitivity by VAS and air blast test at baseline, end of 2 weeks and six weeks salivary calcium and phosphate levels at baseline, 2 weeks and end of 6 weeksTimepoint: Baseline, 2 weeks 6 weeks	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactSangeeta Umesh nayak

Manipal College of Dental Sciences Mangalore

sangeeta.nayak@manipal.edu9880718372

Outcome results