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Effectiveness of Nanohydroxyapetite Paste on Reducing Dentin Hypersensitivity

NCT02936830 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 63

Last updated 2020-03-11

No results posted yet for this study

Summary

The aim of this study is to compare the efficacy of dentine hypersensitivity reduction using in office paste formula containing nanoHydroxyapatite with the commercially available fluoride (duraphat) and a placebo in treating hypersensitivity in a single visit.

Conditions

  • Dentin Hypersensitivity

Interventions

DRUG

5% Sodium Fluoride Varnish

5% sodium fluoride varnish applied on the dentin by the dentist

DRUG

15% Nanohydroxyapetite paste

15% nanohydoxyapetite paste without potassium nitrate or fluoride applied on the dentin by the dentist

DRUG

Glycerol

Glycerol with water in a 1: 1 ratio

Sponsors & Collaborators

  • Riyadh Colleges of Dentistry and Pharmacy

    lead OTHER

Principal Investigators

  • Dalia N AlHarith · Riyadh Colleges of Dentistry and Pharmacy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-31
Primary Completion
2017-03-31
Completion
2017-06-30

Countries

  • Saudi Arabia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02936830 on ClinicalTrials.gov