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临床试验/NCT05187078
NCT05187078已完成不适用

Cervical Bleeding With Cervical Stabilization During IUD Placement: Allis Clamp Versus Single-tooth Tenaculum

Brooke Andrews2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2017年3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
95
试验地点
2
主要终点
Number of patients who experienced bleeding after IUD placement

研究概览

简要总结

This study aims to determine whether an Allis clamp is an effective clamp for cervical stabilization compared to a single-tooth tenaculum.

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)

盲法说明

Physician participants were aware of assignment to utilize the single-toothed tenaculum clamp or allis clamp directly prior to IUD placement procedure. Participants were blinded to the clamp assigned.

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Obtaining IUD

排除标准

  • 未提供

结局指标

主要结局

Number of patients who experienced bleeding after IUD placement

时间窗: At the time of IUD insertion

Number of patients who experienced bleeding after IUD placement with an Allis clamp or single-tooth tenaculum.

次要结局

  • Time to hemostasis(At the time of IUD insertion)
  • IUD insertion success rate(At the time of IUD insertion)
  • Number of interventions required for cervical clamp site bleeding hemostasis(At the time of IUD insertion)
  • Participant reported pain(At the time of IUD insertion)

研究者

发起方
Brooke Andrews
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Brooke Andrews

Resident Physician, OB/Gyn

University of Kentucky

研究点 (2)

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