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临床试验/ACTRN12621000357853
ACTRN12621000357853尚未招募未知

Developing and evaluating a screening tool to improve pre-operative prediction of absence of endometriosis in people with pelvic pain

The Royal Women's Hospital0 个研究点目标入组 666 人开始时间: 2021年3月30日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
666

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
Female

入选标准

  • Women aged 18 – 45 planned to undergo laparoscopy for investigation and/or management of pelvic pain
  • Pelvic ultrasound performed within 12 months of recruitment with no evidence of endometrioma/s and/or deep infiltrating endometriosis
  • oBoth specialist quality and community quality ultrasound included
  • Women with a previous laparoscopy for investigation of pelvic pain and women with a previous diagnosis of endometriosis remain eligible
  • Women with both current and previous hormone use remain eligible

排除标准

  • Unable to provide consent
  • Previous participation in the same study
  • Post-menopausal
  • Pelvic ultrasound showing another likely cause for pain that would independently warrant laparoscopy (eg evidence of tubo-ovarian abscess, hydrosalpinx, other ovarian cyst, fibroid warranting myomectomy).
  • Evidence on ultrasound of endometriosis (endometrioma or DIE)
  • Unable to obtain report of pelvic ultrasound

研究者

发起方
The Royal Women's Hospital

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