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Clinical Trials/TCTR20180611003
TCTR20180611003
Completed
Phase 2

Comparison of efficacy of 5% calcium sodium phosphosilicate and 8% arginine and calcium carbonate in reducing dentin hypersensitivity following non-surgical periodontal therapy

Faculty of Dentistry, Chulalongkorn University0 sites45 target enrollmentJune 11, 2018

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Dentin hypersensitivityChronic periodontitis
Sponsor
Faculty of Dentistry, Chulalongkorn University
Enrollment
45
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 11, 2018
End Date
January 20, 2020
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Faculty of Dentistry, Chulalongkorn University

Eligibility Criteria

Inclusion Criteria

  • The inclusion and exclusion criteria are modified from the guidelines for the design and conduct of clinical trials on dentine hypersensitivity (Holland et al. 1997\)
  • 1\.Adults between 30\-65 years of age
  • 2\.Individual diagnosed with chronic periodontitis
  • 3\.Compliant about at least 2 teeth with DH after receiving at least one visit of scaling and root planing and diagnosed by dentist with air blast (Schiff’s score 2\-3\) or tactile stimulation (VAS sensitivity score more than 4, moderate to severe DH)
  • 4\.Good general health

Exclusion Criteria

  • 1\.Symptom of DH prior to periodontal treatment
  • 2\.Using agents to treat hypersensitivity in the past 3 months
  • 3\.Pharmacotherapeutic histories that may compromise the protocol including the chronic use of anti\-inflammatory, analgesic and mind\-altering drugs
  • 4\.Allergy to either 5% calcium sodium phosphosilicate or 8% arginine and calcium carbonate
  • 5\.DH from dental caries, defective restoration, fractured tooth
  • 6\.Extensively restored teeth and those with restorations extending into the test area
  • 7\.Orthodontic appliance treatment within previous 3 months
  • 8\.Crowded teeth
  • 9\.Abutment teeth for fixed or removable prostheses

Outcomes

Primary Outcomes

Not specified

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