PACTR202309912835123已完成4 期
Comparison of dentofacial and skeletal effects of intermaxillary NiTi coil springs and intermaxillary elastics in the treatment of Class II malocclusion among adolescents.
Dr. Esan Tolulope Bolanle0 个研究点目标入组 48 人开始时间: 2023年8月2日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 48
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 6 Year(s) 至 12 Year(s)(—)
- 性别
- All
入选标准
- •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.
排除标准
- •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.
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