跳至主要内容
临床试验/NCT00534963
NCT00534963已完成不适用

Optimal Catheter Placement During Sonohysterography: A Randomized Clinical Trial Comparing Cervical to Uterine Placement

University of Wisconsin, Madison0 个研究点目标入组 69 人开始时间: 2004年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
69
主要终点
Measure: perceived discomfort

研究概览

简要总结

The primary objective of this investigation was to evaluate if the location of placement of the SIS balloon into either the uterine cavity or the cervical canal affected discomfort perceived during the examination.

详细描述

The use of sonography combined with intrauterine saline instillation, termed sonohysterography

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Participant)

入排标准

性别
Female
接受健康志愿者

入选标准

  • Female patients undergoing SIS for diagnostic uterine cavity evaluation at our university's Reproductive Endocrine Infertility Program.

排除标准

  • previous hysterectomy, current pregnancy, active PID, patulous or stenotic cervical os noted on previous history or physical exam.

结局指标

主要结局

Measure: perceived discomfort

时间窗: during sonohysterography procedure

次要结局

  • Measure: Time required to perform procedure; Measure: Volume of media required to perform procedure(during sonohysterography procedure)

研究者

申办方类型
Other
责任方
Sponsor

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