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NCT03514290
Effect of Low-level Laser Therapy on Post-bleaching Sensitivity and Color Change
NA trial testing Low-lever laser in Tooth Bleaching in 21 participants. Completed in 30 September 2016.
8 August 2016
Quick facts
| Lead sponsor | Universidade Federal do Para |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 21 |
| Start date | 11 July 2016 |
| Primary completion | 8 August 2016 |
| Estimated completion | 30 September 2016 |
| Sites | 1 location across Brazil |
Drugs / interventions tested
- Low-lever laser
- Tooth bleaching — full drug profile →
- Placebo
Conditions studied
- Tooth Bleaching — all drugs for Tooth Bleaching →
- Low-level Laser Therapy — all drugs for Low-level Laser Therapy →
- Dentin Sensitivity — all drugs for Dentin Sensitivity →
- Clinical Trial — all drugs for Clinical Trial →
Sponsor
Universidade Federal do Para — full company profile →
Who can join
Adults 18 to 30, any sex, with Tooth Bleaching or Low-level Laser Therapy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Objective: The objective of this clinical study was to evaluate low-level laser (LLL) therapy in tooth sensitivity and in effecting color change after in-officer bleaching treatment across three weeks of treatment. Methods: Twenty-one volunteers were evaluated through the split-mouth model, so that the right and left maxillary/mandibular quadrants were randomized and allocated to one of two groups: GPLACEBO - the laser tip was positioned without the emission of light (placebo effect) + tooth bleaching with 35% hydrogen peroxide (HP); GLASER - treated with LLL + tooth bleaching with 35% HP. To assess tooth sensitivity, a modified visual analogue scale (VAS) was used after an evaporative stimulus (stimulated pain) and a daily pain questionnaire (unstimulated pain) was also applied. A spectrophotometer was used to measure the color. Three bleaching sessions were performed, with intervals of 7 days. Sensitivity results were tested using Friedman test for intra-group evaluation and Wilcoxon test for inter-group evaluation and ANOVA for color change.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT03514290
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Related trials
Other Universidade Federal do Para trials
Trials by the same sponsor.
- NCT07506850 — Effect of CPP-ACP Associated With NaF or SnF₂ on Post-Bleaching Tooth Sensitivity · NA · completed
- NCT06614764 — Effect of Andiroba on Control of Post-whitening Tooth Sensitivity · NA · completed
- NCT06872749 — Effect of an Experimental Gel Containing Copaiba Oil-resin in the Control of Dentin Hypersensitivity · NA · completed
- NCT06971783 — Effect of an Experimental Gel Based on Acmella Oleracea Extract Associated or Not With Fluoride on Dentin Hypersensitivi · NA · completed
- NCT06518629 — Photobiomodulation Before or After Tooth Whitening · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03514290 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Universidade Federal do Para
- Last refreshed: 2 May 2018
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03514290.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing