NCT02590146已完成不适用
Non-Pharmacologic Patient Centered Pain Control Adjuncts During First Trimester Abortion
University of Hawaii2 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2015年11月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 74
- 试验地点
- 2
- 主要终点
- Difference in overall pain score during procedure between control and intervention group
研究概览
简要总结
This study will examine the use of non-pharmacologic pain control techniques and pain-management counseling as an additional tool for reducing pain during first trimester aspiration abortion.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •English speaking, able to read and understand consent form
- •Age 18 + (minors eligible with parental consent)
- •Seeking in-office aspiration termination of pregnancy
- •Gestational age less than 14 weeks
排除标准
- •Not able to read or understand English
- •Unable to understand consent
- •Minors without parental consent
- •Requesting narcotic or sedative analgesics
- •Currently incarcerated
- •Gestational age greater than 14 weeks
- •Seeking medication abortion
结局指标
主要结局
Difference in overall pain score during procedure between control and intervention group
时间窗: Collected within 1 minute of procedure completion
Patients will complete a visual analog scale to score their overall pain for the procedure.
次要结局
未报告次要终点
研究者
研究点 (2)
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