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临床试验/ACTRN12622000947707
ACTRN12622000947707尚未招募未知

Investigating pRophylactic utErosacral suspension AT Total lAparoscopiC Hysterectomy for patient outcomes and risk of prolapse occurrence - a randomised controlled trial (REATTACH)

Townsville University Hospital0 个研究点目标入组 66 人开始时间: 2022年7月5日最近更新:

试验速览

阶段
未知
状态
尚未招募
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
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
Female

入选标准

  • Patients must be 18 years of age or older
  • Patients must be able to provide informed consent
  • Preoperative inclusion criteria include: C point not past the hymenal remnant, i.e. C point at point 0 at Valsalva
  • Patients with no prolapse symptoms
  • A Pelvic ultrasound scan (USS) in the last 6 months from booking of procedure to show that size of uterus is less than or equal to 300cc

排除标准

  • Women undergoing a total laparoscopic hysterectomy for malignancy
  • Women with a history of pre-existing pelvic organ prolapse, patients with cervical apical descent past the hymen, grade 2 uterocervical pelvic organ prolapse will be excluded
  • Women with serious medical conditions who are unable to perform a Valsalva manoeuvre
  • Non-English-speaking patients (unless access to a qualified interpreter is available during the full duration of the study)
  • Size of uterus on ultrasound scan greater than 300cc
  • Age greater than 75 years old
  • BMI greater than 45
  • Pathology obliterating the pouch of Douglas
  • Stage 4 endometriosis
  • Anticipated geographic relocation within the first 12 months following surgery

研究者

发起方
Townsville University Hospital

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