CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 33 enrolled
Drug / intervention
aligning archwiresother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05391542
NCT05391542N/ACompleted

Effectiveness of Tubular Coaxial Nickel-titanium and Copper Nickel-titanium Orthodontic Aligning Archwires: A Randomized Clinical Trial

University of Baghdad·interventional·Posted May 26, 2022·Updated May 11, 2023

In Brief

A clinical study evaluating aligning archwires for Aligning Archwires. Completed, enrolled 33 participants across 1 site.

Detailed Summary

This study will be done to compare the effectiveness of using coaxial tubular superelastic nickel-titanium and copper-nickel-titanium archwires during the initial phase of orthodontic treatment regarding alignment efficiency, pain perception, and root resorption.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIraq
Collaborators--

Timeline

N/ACompletedFinished
2023202420252026
First PostedMay 26, 2022
Enrollment StartFeb 28, 2022
Primary CompletionOct 15, 2022
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 4.1 years ago

Interventions

aligning archwiresother

At the day of bonding, 0.016-inch archwire will be placed for the TuNT group. Eight weeks later it will be replaced by the 0.018-inch archwire for another eight weeks. While, for the CuNT group, 0.014-inch archwire will be placed at the day of bonding and eight weeks later it will be replaced by the 0.018-inch archwire for another eight weeks. Archwires will be tied to the bracket by elastomeric modules which will be changed every 4 weeks. A good-quality alginate impression for the lower arch should be taken pre-treatment and after 4, 8, 12 and 16 weeks and a stone study model is obtained. Periapical X-ray for the mandibular central incisors will be taken pre-treatment and after 16 weeks. The participants will be provided by a visual analog scale (0-10) to record their pain perception during the first week after each wire placement.