Clinical TrialID 986
Different Concentrations of Potassium Nitrate in In-office Tooth Bleaching Sensitivity
NCT03323372
Tooth Sensitivity
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 986
- Evidence Id
- 986
- Core Evidence Id
- 986
- Source Clinical Trial Id
- 968
- Herb2 Clinical Trial Id
- HBCT000968
- Nct Id
- NCT03323372
- Title
- Different Concentrations of Potassium Nitrate in In-office Tooth Bleaching Sensitivity
- Status
- Completed
- Phase
- Phase 2
- Study Result
- No
- Study Condition
- Tooth Sensitivity
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: PREVENTION
- Intervention
- DRUG: 3% potassium nitrate and 0.25% sodium fluoride|DRUG: 5% potassium nitrate and 2% sodium fluoride
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Triple
- Intervention Purpose
- Prevention
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 56
- Outcome Measure
- absolute risk of tooth sensibility, Patients recorded the occurrence or not of tooth sensitivity (TS) in a sensitivity diary. Participants were asked to register if they experienced DS during treatment and up to 48 hours after bleaching. The Analogic Visual Scale (AVS) was used to assess pain. Each item was scored 0-10 (0- no pain and 10- pain as bad as can be)., 28 days
- Sponsor Collaborator
- Universidade Federal do Amazonas
- Funded By
- OTHER
- Location
- Other Id
- UFAmazonas
- Start Date
- 2016-12-21
- Primary Completion Date
- 2017-05-05
- Completion Date
- 2017-05-20
- First Posted
- 2017-10-27
- Results First Posted
- Last Update Posted
- 2017-10-27
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT03323372
- Title Cn
- Title En
- Different Concentrations of Potassium Nitrate in In-office Tooth Bleaching Sensitivity
- Bilingual Status
- semi_complete