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临床试验/PACTR202404574700044
PACTR202404574700044招募中Unknown

Evaluation of paracervical block versus conscious sedation for pain relief during manual vacuum aspiration: A randomized controlled trial

Emmeh Sweiyi Fiddo0 个研究点目标入组 66 人开始时间: 2024年1月22日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • Women who give consent.
  • Women at less than 13 weeks gestation with incomplete abortion.

排除标准

  • Women with psychiatric or neurological disorders.
  • Women with an allergy to Lignocaine, Pentazocine and/or Diazepam.
  • Women with septic abortion.

研究者

发起方
Emmeh Sweiyi Fiddo

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Evaluation of paracervical block versus conscious... | 临床试验