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Evidence-based prevention of dentine hypersensitivity: A randomized controlled trial to test three interventions

Evidence-based prevention of dentine hypersensitivity: A randomized controlled trial to test three interventions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN80600298
Enrollment
75
Registered
2007-09-28
Start date
2009-02-01
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Oral Health: Dentine hypersensitivity Oral Health Dentine hypersensitivity

Interventions

The three test interventions will be: 1. No treatment 2. Application of a dentine bonding agent 3. Use of a desensitising toothpaste In essence three groups of 25 subjects will be included in the stu

Sponsors

Record Provided by the NHSTCT Register - 2007 Update - Department of Health
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 75 patients with at least one tooth sensitive to hot, cold and sweet stimuli, which does not require any operative treatment (i.e. fillings) will be invited to participate in the study. As part of their routine examination patients will be screened for sensitive teeth according to our protocol. Having had chance to read the patient information leaflet they will then be asked to sign a consent form if they are happy to be included in the study. Inclusion criteria: 1. At least one sensitive tooth. To be eligible subjects will be required to have at least one test tooth sensitive to an evaporative stimulus greater than 40 mm and less than 80 mm on the 100mm visual analogue scale (VAS). 2. Sensitive lesion not requiring restoration 3. Good oral hygiene and gingival health

Exclusion criteria

Exclusion criteria: 1. Under 18 years old 2. Sensitivity resulting from a lesion requiring any form of restoration 3. Sensitivity arising from heavily restored teeth 4. Poor oral hygiene or gingival health

Design outcomes

Primary

MeasureTime frame
Immediate reduction of dental hypersensitivity

Secondary

MeasureTime frame
Prolonged reduction in dental hypersensitivity

Countries

United Kingdom

Outcome results

None listed

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