Comparison of the Prosthesis Ugytex by the Trans-obturator Approach and Anterior Colporrhaphy for the Surgical Treatment of Anterior Vaginal Wall Prolapse
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 162
- 试验地点
- 2
- 主要终点
- number of anatomical recurrences of anterior vaginal wall prolapse of stage 2 or more (POP-Q system)
研究概览
简要总结
Hypothesis / aims of study A RCT has shown that results of prolapse repair via vaginal approach could be improved when a polypropylene mesh is used as tissue support (1). However, non protected heavy-weight meshes were associated with a high rate of local complications such as vaginal erosions and dyspareunia (2). The aim of this multicentre study is to evaluate anatomical and functional results of an innovative low-weight polypropylene mesh protected by an absorbable hydrophilic film in the prolapse repair by vaginal route, in comparison by the standard anterior colporrhaphy.
Study design, materials and methods This study involves 15 centres in French Private or Public Hospital. Patients will be randomly allocated to be operated by a standard anterior colporrhaphy or by an anterior repair reinforced by a specially designed mesh: UgytexTM (Sofradim, France). Ugytex is a low-weight (38g/m²) and highly porous (average porosity: 89%, pores over 1.5mm) polypropylene monofilament mesh offering tissue ingrowth and connective differentiation for a stable and long-term support. The mesh is coated with a hydrophilic film composed of atelocollagen, polyethylene glycol and glycerol. The absorbable coating protects delicate pelvic viscera from the risk of acute inflammation during the healing's inflammatory peak. Prolapse severity will be evaluated using the POP-Q system. In order to evaluate the patient's quality of life, the validated PFDI and the PFIQ questionnaires will be used preoperatively and during follow-up (3), as well as a validated questionnaire on sexual problems. The difference on one-year cure rate should be 15% (80% for the anterior colporrhaphy and 95% for the mesh repair). Then the estimated number of patient is 97 in each arm.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 60 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Patients older than 60 years-old
- •Anterior vaginal wall prolapse of stage 2 or more (POP-Q system)
- •Symptomatic prolapse
- •Informed consent signature obtained
排除标准
- •Patient not able to read French language
- •Patient with a anterior prolapse of stage 1
- •Urinary of vaginal infection
- •Hepatopathy with ascitis
- •Diabetes uncontrolled
- •Treatment by corticosteroids
- •Previous pelvic irradiation
- •Intraoperative bladder injury
结局指标
主要结局
number of anatomical recurrences of anterior vaginal wall prolapse of stage 2 or more (POP-Q system)
时间窗: 1 year
POP-Q score
次要结局
- Perioperative and postoperative morbidity(3 years)
- Rate of local complications of prosthesis (vaginal erosion, prosthesis shrinkage)(3 years)
- Functionnal results following intervention(3 years)
- Post-operative sexuality(3 years)
