跳至主要内容
临床试验/CTRI/2020/06/025715
CTRI/2020/06/025715已完成未知

The role of paracervical block in reducing immediate post operative pain after laparoscopic hysterectomy; a prospective randomised placebo controlled trial

AIIMS New Delhi0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
60

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

入选标准

  • 1.Indication for surgery- benign gynaecological condition
  • 2.Acceptable concomitant procedures- With or without salpingo-oophorectomy, endometrioma excision, ovarian cystectomy
  • 3.Woman giving consent

排除标准

  • 1.Extensive additional tissue manipulation- pelvic lymph node dissection, sacrocolpopexy, anterior/ posterior colporrhaphy, sling surgeries, deep infiltrating endometriosis requiring extensive dissection and excision
  • 2.Gynaecological malignancies
  • 3.Conversion to laparotomy
  • 4.Inability to perform the para-cervical block due to anatomic abnormalities (absent/flush cervix)
  • 5.Known allergy to amide anesthetics
  • 6.Intraoperative inadvertent injury to gastrointestinal or urologic tract that necessitated repair
  • 7.Woman not consenting

研究者

发起方
AIIMS New Delhi

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