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临床试验/NCT01969812
NCT01969812已完成不适用

Patient Satisfaction and Tolerability With the Evie® Slow-Release Insemination Device: Pilot Study

Wake Forest University Health Sciences1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2014年1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
入组人数
22
试验地点
1
主要终点
Patient Tolerability and Satisfaction SF36

研究概览

简要总结

The purpose of this study is to determine patient satisfaction and tolerability of the Evie® slow-release insemination device for US population. Additionally, to assess cramping with the device and to determine pregnancy rates using the slow insemination device compared to standard IUI.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •The inclusion criteria:
  • •Infertile women age ≤39 undergoing first IUI cycle for relatively unexplained infertility
  • •IRB approval and informed consent signed

排除标准

  • •Women <18 or ≥40 years old
  • •Women with abnormalities of the uterine cavity
  • •Women with tubal occlusion
  • •History of documented pelvic adhesions or endometriosis
  • •Uncorrected ovulatory dysfunction
  • •Uncorrected thyroid function
  • •AMH <1 ng/mL
  • •<5 million total motile sperm expected for insemination in prior analyses or on the day of sperm preparation for insemination

研究组 & 干预措施

Evie Slow-Release Insemination Device

Experimental

Preliminary studies in Europe have shown increased pregnancy rates using slow-release insemination. Evie slow-release insemination device is a device that is FDA approved. This device has been used in Europe, it has not yet been used at Carolinas Medical Center, by the Women's Institute. The technique for using this device involves loading a pump syringe with the prepared sperm, placing a balloon-secured catheter and syringe in the patient's sounded uterus, and connecting the insemination syringe to the catheter. The slow-release insemination occurs for 4 hours after the insertion of the catheter. The removal procedure, which can be performed by the patient if desired, involves deflating the catheter balloon and removing the catheter.

干预措施: Evie Slow-release Insemination Device (Device)

Traditional Intrauterine Insemination

Active Comparator

Traditional IUI is one of the treatment modalities for infertility that allows sperm to bypass the cervix and shortens the distance to the fallopian tubes for fertilization. The pregnancy rates for IUI with clomiphene citrate for couples with relatively unexplained infertility have been found to be 7.6% (for women 21-39 years old with up to 3 cycles of IUI with clomiphene).

干预措施: Traditional Intrauterine Insemination (Other)

结局指标

主要结局

Patient Tolerability and Satisfaction SF36

时间窗: 1 month

The primary outcome variable will be patient tolerability and satisfaction, based on a standardized SF-36 survey. Total score 0-100 with higher score denoting better outcomes

次要结局

  • Cramping(1 month)
  • Pregnancy Rates(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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