Skip to content

In-vivo comparison study of the effectiveness of three different toothpastes in reduction of dental hypersensitivity

In-vivo comparison study of the effectiveness of three different toothpastes in reduction of dental hypersensitivity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014839
Enrollment
99
Registered
2018-11-08
Start date
2018-11-15
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

Hypersensitivity

Interventions

Group 1: The participants are distributed with the toothpaste "Sensodyne repair and protect" as well as a toothbrush. Both are to be used throughout the clinical trial. In the beginning as well as aft

Sponsors

Förderverein Universität Witten/ Herdecke
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: adults (18 yrs+), availability during the 4 weeks of the trial, at least one hypersensitive tooth, with a Schiff cold air scale score of two or higher. No use of desensitizing measures since one month prior the beginning of the trial. A minimum of 10 remaining teeth, except wisdom teeth, without a crown, partial crown or large restoration. A written consent of the patient after succeeded elucidation. The Patient is capable of grasping the content and circumstances of the clinical trial and neither in the middle of a dental treatment nor ridden by relevant oral diseases (e.g. tooth pain, diseases of the mucosa, etc.)

Exclusion criteria

Exclusion criteria: Suspection of incapability to keep up with the test plan, severe overall diseases, pregnancy or breastfeeding period. Persistent calculus, use of antibiotics or anti-inflammatories within two weeks prior to the beginning of the trial, necessary antibiotic prophylaxis, hypersensitive teeth with a mobility higher than 1, dental bleeching within two months prior to the trial, bad oral hygiene, use of anti-inflammatory or pain relieving drugs throughout the trial, oral diseases, e.g. NUG, NIJP, deseases of the immune system e.g. HIV, hepatitis, tuberculosis, known hypersensitivity towards substances used within the clinical trial, current participation in a different clinical trial

Design outcomes

Secondary

MeasureTime frame
evaluation of tooth hypersensitivity after thermal irrigation after one and after four weeks

Primary

MeasureTime frame
evaluation of tooth hypersensitivity after tactile irrigation after one and after four weeks

Countries

Germany

Contacts

Public ContactTim Michalski

Abteilung für präventive Zahnmedizin Universität Witten/Herdecke

tim.michalski@uni-wh.de017622375579

Outcome results

None listed

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