Viewing Study NCT04367324



Ignite Creation Date: 2024-05-06 @ 2:36 PM
Last Modification Date: 2024-10-26 @ 1:33 PM
Study NCT ID: NCT04367324
Status: COMPLETED
Last Update Posted: 2020-05-01
First Post: 2020-04-24

Brief Title: Effect of Low-Level Laser Therapy Following Direct Pulp Capping on Postoperative Sensitivity by Thermal Stimulus
Sponsor: TC ORDU ÜNİVERSİTESİ
Organization: TC ORDU ÜNİVERSİTESİ

Study Overview

Official Title: Effect of Low-Level Laser Therapy Following Direct Pulp Capping on Postoperative Sensitivity by Thermal Stimulus A Retrospective Study
Status: COMPLETED
Status Verified Date: 2020-04
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: The aim of this study was to investigate the effect of low-level laser therapy LLLT on postoperative pain provoked by thermal stimulation in direct pulp capping All the patients who received consent form in this retrospective study were retrieved from the records of patients attended for routine dental treatment at the Ordu University Faculty of Dentistry Department of Endodontics between 01102017-01102018 Study subjects were recruited from the pool of patients who performed direct pulp capping by a single operator A total of 123 pre-treated teeth of 123 patients who referred to Ordu University Faculty of Dentistry were examined Follow-up examinations were carried out at postoperative 6th hours 1st and 7th days with visual analog scale VAS and treatment outcome were assessed Participants were allocated to the laser and control group which consist of 42 patients in each group 6 patients were excluded from the study due to missing data in both groups Thus data from 72 patients who had been carried out direct pulp capping were assessed
Detailed Description: None

Study Oversight

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