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Comparison of clinical efficacy of continuous coaxial wire with NiTi overlay method in treatment management of high-buccal canines

Comparison of clinical efficacy of continuous coaxial wire with NiTi overlay method in treatment management of high-buccal canines : Clinical Trial Study

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250919067290N1
Enrollment
36
Registered
2025-10-19
Start date
2025-11-22
Completion date
Unknown
Last updated
2025-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High buccal maxillary canine.

Interventions

Intervention 1: Intervention group: In the first group, a 0.155 coaxial wire (DB orthodontics, Silsden, United Kingdom) will be used to straighten and flatten the teeth, and the buccal canine will als

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: Individuals between the ages of 12 and 18 Individuals with a permanent dentition Individuals with at least one high buccal canine which incisal edge is at least 4 mm more gingivally than the adjacent lateral incisal edge Individuals who are in grades 0 and 1 in terms of hygiene based on the Silness & Loe index Individuals who are candidates for fixed orthodontic treatment with a treatment plan to extract the upper first premolars No metabolic problems or taking medications that affect bone metabolism No posterior crossbite

Exclusion criteria

Exclusion criteria: need for segmental techniques from the beginning of treatment for canine retraction and correction Failure to visit and follow up with individuals

Design outcomes

Primary

MeasureTime frame
Maxillary second premolar tooth position measurements. Timepoint: At the beginning of the study (before the intervention) and at the end of treatment. Method of measurement: Geomatic x control software.;Maxillary lateral tooth position measurements. Timepoint: At the beginning of the study (before the intervention) and at the end of treatment. Method of measurement: Geomatic x control software.

Secondary

MeasureTime frame
BOP. Timepoint: At the beginning of the study (before the intervention) and at the end of treatment. Method of measurement: In clinic with a periodontal probe.;Time. Timepoint: At the end of treatment. Method of measurement: Time interval from the start of the intervention until the canine tooth comes into arch.;Pain. Timepoint: In the overlay intervention group, both after initial archwire placement and after canine engagement, in the coaxial intervention group, after initial archwire placement. Method of measurement: Visual analogue scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactErfan Shadi

Mashhad University of Medical Sciences

Shadie4031@mums.ac.ir+98 51 3846 7343

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026