Viewing Study NCT06526871



Ignite Creation Date: 2024-10-26 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 3:36 PM
Study NCT ID: NCT06526871
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-19

Brief Title: Evaluation of Treatment Outcome of Lower Incisors Crowding Using Clear Aligners With Laser Acceleration
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of Treatment Outcome of Lower Incisors Crowding Using Clear Aligners With Laser Acceleration Randomized Control Study
Status: COMPLETED
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The present study will be performed to evaluate the effect of low-level laser therapy LLLT on the rate of orthodontic tooth movement through the correction of lower incisors crowding using clear aligners
Detailed Description: This study will employ a two-arm parallel randomized clinical trial design with an allocation ratio of 11 The study will include participants aged 16 to 23 years with mild to moderate anterior lower crowding and Class I Angle malocclusion presenting with a full set of teeth excluding wisdom teeth Eligible participants will be randomly assigned to either the intervention group receiving LLLT in addition to clear aligner therapy or the control group receiving clear aligner therapy alone

Intervention

The intervention group will undergo LLLT using the Biolase Epic X device calibrated to 02 W power 016 J energy and 08 seconds pulse duration per point The laser will be applied to five points on the buccal surface cervical mesial distal middle root apical mesial and distal and four points on the lingual surface cervical mesial distal middle root and middle apical of the target tooth LLLT sessions will be conducted weekly over seven sessions

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