Viewing Study NCT06324162



Ignite Creation Date: 2024-05-06 @ 8:17 PM
Last Modification Date: 2024-10-26 @ 3:24 PM
Study NCT ID: NCT06324162
Status: COMPLETED
Last Update Posted: 2024-03-21
First Post: 2024-03-03

Brief Title: Does the Pain Experienced During Orthodontic Treatment and Bracket Removal Depend on the Architecture of the Bracket
Sponsor: Piotr Fudalej
Organization: Jagiellonian University

Study Overview

Official Title: Does the Pain Experienced During Orthodontic Treatment and Bracket Removal Depend on the Architecture of the Bracket A Comparative Study of Two Bracket Systems and Two Debonding Methods
Status: COMPLETED
Status Verified Date: 2024-03
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: Debonding
Brief Summary: The present research aimed to thoroughly investigate the impact of bracket architecture on pain perception during active treatment debonding and adhesive removal
Detailed Description: 100 consecutive patients who completed treatment with one of two bracket systems 2-slot brackets with integral base or conventional twin brackets with foil mesh were included in this prospective clinical trial Prior to the removal of brackets participants were asked to evaluate the level of pain encountered throughout their orthodontic treatment with the fixed appliances utilizing a 0-10 numerical rating scale and to indicate the main cause of pain Subsequently brackets on the right side of both dental arches were debonded using the lift-off debonding instrument LODI while on the left side the bracket removal pliers BRP The residual adhesive was removed through two methods manual in the upper arch and rotary in the lower The same scale was employed to assess pain levels during brackets and adhesive removal

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