Efficacy of two different dentinal hypersensitivity reducing mouth rinses in patients with pain caused by professional tooth cleaning-single-blind, randomized, controlled, clinical study

Not Applicable

• Conditions: Dentin Hypersensitivity; K08; K03.8; Other disorders of teeth and supporting structures; Other specified diseases of hard tissues of teeth

• Registration Number: DRKS00010811
• Lead Sponsor: Abteilung der Zahnerhaltung und Parodontologie der Zahnklinik Uni Köln

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-06-27
• Study Completion: 2018-04-02
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 155

Inclusion Criteria

To be eligible, a patient must comply with all of the following criteria:
1)Age range: at least 18 years (>1996)
2)Written informed consent
3)periodontal maintenance or dental prophylaxis patient
4)Recall frequency twice a year (or more)
5)Recall appointment third or more

Exclusion Criteria

• requiring treatment carious lesions
• antibiotic therapy (up to 7 days prior to study entry)
• Long time medicamentation with analgesics or anti-inflammatory drugs
• Allergies against mouthwashes or their ingredients used
• Pregnant and lactating women
• Expected unavailability for the period of study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The pain during the professional cleaning of the teeth is measured by means of a questionnaire according to the PZR, which is measured via Visual Analog Scale (in mm) and Visual Reading Scale (in words)

Secondary Outcome Measures

Name	Time	Method
Quality of life and adherence to the product, as well as general information about the products used, will be determined by questionnaires. Safety will be documented by oral examination