ANSiStim Study for Active Labor Pain (ANSS-ALP)
Study of ANSiStim for Pain Relief During Active Labor Phase Through Continues Checking of VAS SCORE
研究概览
详细说明
研究类型
注册 (预期的)
阶段
- 不适用
联系人和位置
学习地点
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Karnataka
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Bangalore、Karnataka、印度、560 076
- 招聘中
- Fortis Hospital
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接触：
- Gayathri D Kamath, M.D.
- 电话号码：91-80-6621 4444
- 邮箱：enquiries@fortishealthcare.com
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接触：
- Jithesh R P, M.B.A.
- 电话号码：917708931316
- 邮箱：r.p.jithesh@dyansys.com
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Pregnant Women on an Active Labor
Exclusion Criteria:
- Cardiac Pacemaker or any other implants
- Psoriasis
- Diminish mental capacity
学习计划
研究是如何设计的？
设计细节
- 主要用途：支持治疗
- 分配：不适用
- 介入模型：单组作业
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的：ANSiStim
The ANSiStim device is designed to administer auricular point stimulation treatment over several days. The advantage of using the ear for this treatment is that it provides numerous points for stimulation within a small area. Stimulation is performed by electrical pulses emitted through strategically positioned needles. Three zinc air batteries with 1.4 V provide the required stimulation energy for 96 hours. This constant current source guarantees equivalent stimulation energy regardless of the individual impedance of the skin. The treatment period varies based on the severity of the pain. To minimize the risk of adaption or tolerance to the electrical stimulation, it is applied for 3 hours, followed by a pause of 3 hours. |
ANSiStim allows continuous point stimulation over a period of several days while offering the patient a high degree of comfort and mobility at the same time.
Use of the ANSiSTIM therapy provides overwhelming advantage over drug therapy minimizing possible side-effects caused by pain medications (i.e.
opioid) such as, for example, impaired reactions.
In most cases, the patient continues to lead its life as normal, without side effects or any loss of quality of life.
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研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Evidence of Reduced Pain (Pain Scale of 5) in Active Labor Phase after ANSiStim Placement
大体时间：48 Hours
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48 Hours
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合作者和调查者
调查人员
- 首席研究员：Gayathri D Kamath, M.D.、Fortis Hospital - Bangalore
研究记录日期
研究主要日期
学习开始
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.