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Clinical Evaluation for Post Bleaching Hypersensitivity Using Desensitizing Agent During In-office Bleaching

Clinical Evaluation for Post Bleaching Hypersensitivity Using Desensitizing Agent Before and /or After In-office Bleaching

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02942082
Enrollment
36
Registered
2016-10-21
Start date
2017-11-01
Completion date
2018-11-29
Last updated
2019-09-18

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

Conditions

Tooth Bleaching

Brief summary

Evaluating the effect of a desensitizing agent on post-bleaching hypersensitivity.

Detailed description

A randomized clinical trail will be done to evaluate the effect of a desensitizing agent ACP oral care gel in comparison to a control group on hypersensitivity after bleaching using a visual analogue scale.

Interventions

OTHERACP oral care gel

a desensitizing agent will be applied on tooth before and/or after bleaching

OTHERglycrin

glycrin will be applied on tooth surface before and/or after bleaching

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients must show no signs of spontaneous dental pain. * Male or female patients between the ages of 18 to 40. * Patients with good general and oral health. * Patients having six caries-free maxillaryanterior teeth without restorations on the labial surfaces. * Patients should have central incisors determined to be shade C2 or darker

Exclusion criteria

* Patient with spontaneous dental pain. * Patient with anterior restorations or non carious cervical lesion. * Patient having severe internal tooth discoloration (tetracycline stains, fluorosis, pulpless teeth), and bruxism habits. * Tempro-mandibular joint problems involving symptomatic pain. * Patients taking analgesics that could alter their normal pain perception level. * Pregnant or breast feeding women.

Design outcomes

Primary

MeasureTime frameDescription
Post-bleaching hypersensitivity assessed using visual analogue scaleone monthusing visual analogue scale

Secondary

MeasureTime frameDescription
Tooth color assessed using value-ordered VITA® Classical Shade Guideone monthvalue-ordered VITA® Classical Shade Guide

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026