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Comparing the effects of Nickel Titanium (NiTi) coil springs and elastics on the dental skeletal and soft tissues in patients on braces.

Comparison of dentofacial and skeletal effects of intermaxillary NiTi coil springs and intermaxillary elastics in the treatment of Class II malocclusion among adolescents.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
PACTR
Registry ID
PACTR202309912835123
Enrollment
48
Registered
2023-09-28
Start date
2021-08-02
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Oral Health

Interventions

Class II elastics
Class II NiTi coil springs.

Sponsors

Dr. Esan Tolulope Bolanle
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Class II Molar and/or canine relationship with at least half unit cusp disto-occlusion on one or both sides of the jaw. 2. Subjects aged 10-19years old 3. Presence of all permanent teeth up to first molar 4. Minimum overjet of 5mm 5. Subjects with complete pre-treatment records which are lateral cephalometric radiograph, study models and clinical photographs. 6. Subjects who have completed the levelling and alignment phase of non-extraction fixed orthodontic therapy with Roth 0.022 prescription and are on upper and lower 0.019x0.025-inch Stainless steel wires. 7. Subjects between 10-15years must give assent (Appendix 2) and subject’s parent must give consent. While subjects between 16-19years must give consent.

Exclusion criteria

Exclusion criteria: 1. Subjects with syndromic or craniofacial abnormalities such as cleft lip and palate. 2. Subjects with missing permanent tooth not including second and third molars. 3. Subjects with missing or incomplete records. 4. Subjects with springs that showed permanent deformation at any of the recall visits. 5. Subjects allergic to latex and nickel titanium. 6. Subjects on routine medications such as contraceptives, bisphosphonates or non-steroidal anti-inflammatory drugs (NSAIDs). 7. Subjects not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
Changes in skeletal, Dental, and soft tissues in Class II malocclusion

Secondary

MeasureTime frame
OHRQoL between both groups using OHIP-14

Countries

Nigeria

Contacts

Public ContactTolulope Esan

Senior Registrar

tolulope_esan@yahoo.com08090365545

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026