CTRI/2022/09/045312已完成未知
Comparison of safety and efficacy of 2 brands of Botulinum Toxin A for the treatment of crow’s feet: A Split face study
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 50
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
入选标准
- •18 years and above
- •Both Male and Female
- •Moderate to severe lateral canthal lines associated with orbicularis oculi activity
排除标准
- •a)Known Hypersensitivity to Botulinum Toxin
- •b)Subjects with neuromuscular disorders (myasthenia gravis, Lambert-Eaton myasthenic syndrome, amyotrophic lateral sclerosis, or motor neuropathy)
- •c)Subjects who used medications that interfere with the neuromuscular function, such as aminoglycoside antibiotics and curare-like agents, within 4 weeks before screening.
- •d)Subjects with a previous injection of botulinum toxin Type A within 3 months or cosmetic procedures associated with crow’s feet
- •e)Pregnancy and lactation
研究者
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