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Study to know the effectiveness of three toothpastes Hydent Pro, Vantej and Thermoseal Repair for the treatment of teeth sensitivity

Comparative Effectiveness of Fluoro Calcium Phosphosilicate, Calcium Sodium Phosphosilicate, and Strontium Chloride Hexahydrate containing Toothpastes for the Treatment of Dentin Hypersensitivity â?? A Randomized Single Blind study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/04/013481
Enrollment
93
Registered
2018-04-25
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

Health Condition 1: null- Dentin Hypersensitivity Health Condition 2: K038- Other specified diseases of hard tissues of teeth

Interventions

Intervention1: Fluoro Calcium Phosphosilicate bioactive glass (BioMin�) containing desensitizing toothpaste (Hydent Pro®): Subjects will be dispensed allocated test tooth paste at baseline visit to

Sponsors

Dr Shalini Agarwal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a. Volunteers who are aged 18-50 years b. Presenting at least 1 tooth with diagnosed dentin hypersensitivity (Painful response to dental explorer) and VAS score at baseline of at least 5 for the sensitive teeth c. Volunteers with good general and oral health and acceptable hygiene as determined by clinical investigator d. Willingness to participate in the study and able to provide written and oral informed consent.

Exclusion criteria

Exclusion criteria: a. Systemic illness and/or dental emergency condition needing urgent treatment b. Severe generalized periodontitis. c. Non-surgical or surgical therapy for periodontitis within last 12 months d. Presence of active caries, cracks, fractures in cervical areas of affected teeth e. Restorations, prosthesis, orthodontic appliances involving cervical areas of affected teeth. f. Ongoing use of analgesics, anti-inflammatory or anti-histaminic agents g. Use of other home-care desensitizing toothpastes or in-office treatments within 8 weeks h. Self-reported pregnancy or nursing i. Current self-reported drug or alcohol dependence j. Non-willingness to participate.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure for assessment of pain will be VAS score in response to test stimuli. VAS has been validated and tested for reliability for measuring clinical and experimental pain.Timepoint: During treatment period

Secondary

MeasureTime frame
The secondary outcome measure for pain; VRS score has good correlation with alternative pain assessment tools and has an advantage of patient compliance.Timepoint: During treatment period

Countries

India

Contacts

Public ContactDr Shalini Aggarwal

Dr. D Y Dental College and Hospital

shalini.aggarwal@dpu.edu.in

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 22, 2026