跳至主要内容
临床试验/EUCTR2004-005138-38-DK
EUCTR2004-005138-38-DK进行中(未招募)不适用

Antibiotikaprofylakse ved vaginalplastik

Hvidovre Hospital0 个研究点目标入组 200 人开始时间: 2005年1月17日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Women age +18 with uterine prolapse grade I-II and/or cystocele and/or rectocele and/or enterocele grade I - IV and/or defects of the perineal body, in whom there is medical indication for vaginal repair, but no indication for vaginal hysterectomy or transvaginal suspension of the vaginal vault after prior hysterectomy.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients allergic to Cefuroxim.
  • Patients in whom a vaginal hysterectomy or a transvaginal suspension of the vaginal vault or other major surgery is planned, where prophylactic antibiotic treatment is standard.
  • Patients suffering from physical or mental disorders that will not allow them to give informed consent.
  • Pregnant and nursing women.
  • Drop outs are defined as:
  • Patients where the surgeon find it indicated to perform a VH or VV-suspension, or laparotomy, where prophylactic antibiotic treatment is standard.
  • Patients with adverse events. I.e. intraoperative bladder, ureter or bowl injury where antibiotics are obligatory.

研究者

相似试验

Antibiotikaprofylakse ved vaginalplastik | 临床试验