ISRCTN12229381进行中（未招募）Unknown
Exploring the feasibility and acceptability of conducting a study comparing the effectiveness of colpocleisis with sacrospinous fixation in women with pelvic organ prolapse (the C-POP study)
试验速览
- 阶段
- Unknown
- 状态
- 进行中（未招募）
- 入组人数
- 100
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
- 性别
- All
入选标准
- •1. Female (or assigned female at birth)
- •2. Age 18 years and above
- •3. Diagnosed with apical pelvic organ prolapse
- •4. Eligible for both colpocleisis and SSF procedures (or have already had one or both surgeries previously)
- •5. Ability to provide informed consent
- •6. Able to communicate in either English, Polish, Urdu, Punjabi or Welsh
- •1. UK-based secondary care healthcare professionals involved in the care of women with apical pelvic organ prolapse (either currently or within the last 5 years)
- •2. Working in a UK complex uro-gynaecology centre
- •3. Able to give informed consent and speak English
- •1. Females (or those assigned female at birth)
- •2. Age 18 years and above
- •3. Diagnosed with apical pelvic organ prolapse
- •4. Eligible for both colpocleisis and SSF procedures (i.e., no longer intend to have penetrative vaginal intercourse and who are willing to have either surgical procedure)
- •1. Women as per WP1
- •2. Healthcare professionals as per WP2
- •3. Other stakeholders who might be involved in a future effectiveness trial, can converse in English, and who can give informed consent
排除标准
- •WP1: There are no exclusion criteria
- •WP2: HCPs based in primary care
- •WP3: There are no exclusion criteria
- •WP4: There are no exclusion criteria
研究者
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