跳至主要内容
临床试验/DRKS00014232
DRKS00014232招募中不适用

Evaluation of pre-surgical high resolution magnetic resonance imaging (MRI) compared to post-surgical MRI results of mesh-repair surgery in women with pelvic organ prolapse (implantation of polypropylene synthetic grafts). - VisiTexKAB

niversitätsfrauenklinik Heidelberg0 个研究点目标入组 50 人开始时间: 2018年3月5日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50

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 one(—)
性别
Female

入选标准

  • female pelvic organ prolapse (cystocele, rectocele, uterine prolapse), symptomatic pelvic floor disorder, quality-of-life impairment, planned pelvic floor reconstructive surgery with alloplastic material (including MR-visible meshes), >18 years of age, female, no history of repair surgery with alloplastic material in the anamesis, written informed consent.

排除标准

  • contraindication against MRI, age belo 18, no written informed consent

研究者

发起方
niversitätsfrauenklinik Heidelberg

相似试验