Comparison of the anti-sensitivity effects of Poneh and Sensodyne dentifrices

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT138903291150N3

Enrollment

150

Registered

2012-12-07

Start date

2010-11-27

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Hyper sensitivity of dentine. Other specified diseases of hard tissues of teeth

Interventions

Intervention 1: Intervention in test group: prescription an Iranian antisensitive dentifrices (Poneh) contain 10% Potassium nitrate twice in day for 1 month. Intervention 2: Intervention in control gr

Treatment - Drugs

Intervention in test group: prescription an Iranian antisensitive dentifrices (Poneh) contain 10% Potassium nitrate twice in day for 1 month

Intervention in control group: prescription a Foreign antisensitive dentifrices (Sensodyne) contain 5% Stransium Chloride twice in day for 1 month

Eligibility

Sex/Gender

All

Age

25 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 25-35 years; patients who have more than 3 hypersensitive teeth; teeth must be vital. Exclusion criteria: systemic diseases; using any drugs like antihistamine, sedative ,anti-inflammatory, anti-hypertension, local antisensitive, during the research period; using any antisensitive method for their teeth for last 3 months; teeth in investigation area with any enamel caries, deep cervical restorations; teeth in investigation area with fixed prosthesis; abudment and mobility grade more than 1 degree; pregnancy; breastfeeding period; allergy to potassium nitrate; extensive cervical caries; those who had allergy to experimental dentifrice and who had nonvital teeth; smokers.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Hyper sensitivity of dentine. Timepoint: After first, second week and also in second and third months. Method of measurement: 4 instruments used for measurement of primary outcome, all of them used for production a contact stimuli for indicating the level of hypersensitivity, such as: 1- Williams probe, 2- ice in contact with buccal surface of the teeth for about 3 seconds, 3- unit compressed air, 4- unit water with about 20 centigrade.	—

Measure

Time frame

Hyper sensitivity of dentine. Timepoint: After first, second week and also in second and third months. Method of measurement: 4 instruments used for measurement of primary outcome, all of them used for production a contact stimuli for indicating the level of hypersensitivity, such as: 1- Williams probe, 2- ice in contact with buccal surface of the teeth for about 3 seconds, 3- unit compressed air, 4- unit water with about 20 centigrade.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMr. Ahmadian

Goltash company

ahmadian@goltash.com+98 33 5537 3350

Outcome results

None listed

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