Viewing Study NCT06066671



Ignite Creation Date: 2024-05-06 @ 7:35 PM
Last Modification Date: 2024-10-26 @ 3:10 PM
Study NCT ID: NCT06066671
Status: COMPLETED
Last Update Posted: 2024-05-08
First Post: 2023-09-27

Brief Title: The Effect of an Experimental Gel Based on Copaiba Oil Resin in Reducing Post-bleaching Tooth Sensitivity
Sponsor: Universidade Federal do Para
Organization: Universidade Federal do Para

Study Overview

Official Title: Evaluation of the Effect of na Experimental Gel Based on Copaiba Oil Resin in Reducing Post-bleaching Tooth Sensitivity a Randomized Clinical Study
Status: COMPLETED
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This randomized double-blind clinical trial aimed to evaluate the effect of an experimental gel containing copaiba oil resin in reducing postoperative tooth sensitivity caused by bleaching with 35 hydrogen peroxide The volunteers of this study were randomized into 3 different groups - GC placebo GN potassium nitrate and sodium fluoride GCO copaiba oil resin The dental elements of the GCO received application of the experimental desensitizing gel on the buccal surfaces of the central incisors lateral incisors canines and upper and lower premolars with a rubber cup in an active way for 10 minutes The GC and GN groups also received the application of a placebo gel and a nitrate potassium and sodiun fluoride gel respectively under the same conditions described for the experimental gel Subsequently all groups underwent in-office bleaching treatment with 35 hydrogen peroxide Post-bleaching sensitivity was collected through a form composed of the visual analogue scale VAS Color measurement was performed at two times baseline Ti and one week after the 3rd bleaching session Tf
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None