Actively Recruiting
Clinical Performance of the I-arch System During the Initial Stage of Orthodontic Treatment
Led by Tabark H. Omran · Updated on 2026-04-22
34
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
T
Tabark H. Omran
Lead Sponsor
U
University of Baghdad
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if the I-arch system works to align the moderately misaligned teeth in patients seeking orthodontic treatment. it aims to answer the following questions: * Does I-arch system increase the rate of teeth alignment? * Does I-arch system produce significant changes in arch width and incisors inclination? * Does I-arch system decrease the intensity of patient-reported pain and root resorption? Researchers will compare the effectiveness of the I-arch and MBT arch wire system.
CONDITIONS
Official Title
Clinical Performance of the I-arch System During the Initial Stage of Orthodontic Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Moderate crowding of mandibular anterior teeth (3-6 mm) according to Little's irregularity index in patients aged 12 years or older
- Full set of permanent teeth present except third molars
- Brackets placed on maxillary and mandibular anterior teeth without interference from overbite or overjet
- Maxillary and mandibular incisors without prior trauma or root resorption
You will not qualify if you...
- History of previous orthodontic treatment
- Severe crowding of mandibular and maxillary anterior teeth greater than 6 mm (Little's irregularity index)
- Presence of teeth severely misaligned out of the dental arch and unable to be engaged with aligning arch wire
- Presence of periodontally compromised teeth or previous loss of attachment
AI-Screening
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Trial Site Locations
Total: 1 location
1
AlHur ALriyahi and Hai Alhussein specialized dental centerS
Karbala, Iraq
Actively Recruiting
Research Team
T
Tabark H. Omran
CONTACT
P
Prof. dr. Yassir A. Yassir, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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