Clinical TrialID 983

Potassium Nitrate and Post-bleaching Sensitivity

NCT03523598

Medicaments Substances in Therapeutic Use

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Record Fields

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Clinical Trial Id
983
Evidence Id
983
Core Evidence Id
983
Source Clinical Trial Id
965
Herb2 Clinical Trial Id
HBCT000965
Nct Id
NCT03523598
Title
Potassium Nitrate and Post-bleaching Sensitivity
Status
Completed
Phase
Study Result
No
Study Condition
Medicaments Substances in Therapeutic Use
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Intervention
OTHER: Placebo gel + Normal Toothpaste|OTHER: Placebo Gel + Potassium Nitrate Toothpaste|OTHER: Potassium Nitrate Gel + Normal Toothpaste
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult
Enrollment
75
Outcome Measure
Risk to the tooth sensitivity (VAS), The tooth sensitivity will be assessed using a Visual analogue (VAS) scale. VAS consisted of a 10-cm scale 0 (no sensitivity) 10 (unbearable sensitivity). A slightly air-stream will be applied over the buccal surfaces of the central incisors, and the patients will record their sensitivity perception by pointing with a pen on the scale. The distance between the marking and the border of scale, relative to the absence of sensitivity will be measured. The measurements will be scored according to the distance from 0, using a digital caliper. The risk of tooth sensitivity will be determined by relative risk assessed by ratio between absolute risk of experimental condition by those observed in control. The 95% confidence interval will be calculated., During the bleaching treatment|Risk to the tooth sensitivity (VRS), The tooth sensitivity will be evaluated using a 5-point Verbal rating scale (VRS), where 0 = none, 1 = mild, 2 = moderate, 3 = considerable and 4 = severe. Score different from 0 will determine presence of sensitivity.The risk of tooth sensitivity will be determined by relative risk assessed by ratio between absolute risk of experimental condition by those observed in control. The 95% confidence interval will be calculated., During the bleaching treatment
Sponsor Collaborator
Universidade Federal de Sergipe|Johnny Alexandre Oliveira Tavares
Funded By
OTHER
Location
Federal University of Sergipe, Aracaju, Sergipe, 49060-108, Brazil
Other Id
UFSergipe.
Start Date
2018-05-26
Primary Completion Date
2018-06-01
Completion Date
2018-09-01
First Posted
2018-05-14
Results First Posted
Last Update Posted
2020-08-12
Study Document
Study Url
https://clinicaltrials.gov/study/NCT03523598
Title Cn
Title En
Potassium Nitrate and Post-bleaching Sensitivity
Bilingual Status
semi_complete