NCT01819051已完成不适用
A Single Center, Pilot Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of the Plasma Treatment System in Treating Onychomycosis
Moe Medical Devices1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2013年3月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Change in number of reported adverse events
研究概览
简要总结
The purpose of this study is to evaluate the safety of treating human toenails with atmospheric plasma (MOE Antimicrobial Plasma Treatment System) and get an initial evaluation of the efficacy of this treatment for toenail fungus (onychomycosis).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Subject must be between 18 and 75 years of age inclusive, of either sex, and of any race;
- •Subject must have distal subungual infection that affects approximately 25% to 50% of at least one great toenail, both clinically and mycologically diagnosed;
- •Subject must have at least 2 mm of the proximal end of the target toenail free of infection;
- •Subject must have a target toenail that is assessed as capable of growing approximately 1 mm/month, (e.g., the subject needs to report cutting his or her toenails at least once per month);
- •Subject must be willing to give written informed consent and able to adhere to procedures and visit schedules;
- •Woman of childbearing potential who is currently sexually active must agree to use a medically accepted method of contraception while receiving protocol-specified medication and for 30 days after stopping the medication. Methods include condoms (male or female) with or without a spermicidal agent, diaphragm or cervical cap with spermicide, medically prescribed intrauterine device, oral or systemic hormonal contraceptive (plus an additional reliable barrier method), and surgical sterilization (e.g., hysterectomy or tubal ligation).
- •Woman of child-bearing potential who is not currently sexually active must agree to use a medically accepted method of contraception should she become sexually active while participating in the study.
- •Woman of childbearing potential must have a negative serum pregnancy test within 72 hours prior to start of study drug.
排除标准
- •Subject with one or more of the following conditions on the target toenail:
- •proximal subungual onychomycosis,
- •white superficial onychomycosis,
- •dermatophytoma or "yellow spike/streak",
- •exclusively lateral disease,
- •inability to become normal in the opinion of the investigator.
- •Subject with psoriasis, severe moccasin-type tinea pedis requiring treatment, symptomatic interdigital tinea pedis, lichen planus, or other abnormalities that could result in a clinically abnormal nail;
- •Subject with peripheral vascular disease or peripheral circulatory impairment;
- •Subject with history of uncontrolled diabetes mellitus;
- •Subject with known chronic or active liver disease;
- •Subject with any known immunodeficiency;
- •Any pacemakers, or any metallic implants or prostheses in the vicinity of the treatment site (such as ankle, foot, etc.).
- •Subject with any clinically significant condition or situation, other than the condition being studied that, in the opinion of the investigator, would interfere with study evaluations or optimal participation in the study;
- •Subject who has received systemic antifungal therapy within 6 months or topical antifungal therapy applied to the foot or toenails within 1 month of study entry;
- •Subject who has received radiation therapy, chemotherapy, and/or immunosuppressive drugs within 6 months of study, and/or oral corticosteroids for >1 month within the 6 months of study (exception: inhaled steroids);
- •Subject known to have received treatment with investigational drugs within 30 days prior to enrollment into this study;
- •Subject who is unable to communicate or cooperate with the investigator due to language problems, poor mental development, or impaired cerebral function
- •Subjects who may be unreliable for the study including subjects who engage in excessive alcohol intake or drug abuse (no testing required), or subjects who are unable to return for scheduled follow-up visits
- •Woman who is breastfeeding, pregnant, or intends to become pregnant;
- •Subject who is part of the staff personnel directly involved with this study;
- •Subject who is a family member of the investigational study staff.
研究组 & 干预措施
Plasma
Experimental
Apply plasma to great toenail for up to 20 minutes, 1X/week for 3 weeks
干预措施: MOE Antimicrobial Plasma Treatment System (Device)
结局指标
主要结局
Change in number of reported adverse events
时间窗: Change from Baseline to 6 months post-treatment
次要结局
未报告次要终点
研究者
研究点 (1)
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