ACTRN12608000109303已完成未知
A comparative, single-blind, randomised trial of pain and ultrasound estimation of residual pelvic fluid associated with suction or non-suction drains following gynaecological laparoscopy
Department of Endo-Gynaecology0 个研究点目标入组 180 人开始时间: 2008年2月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 180
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
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 80 Years（—）
- 性别
- Female
入选标准
- •Women undergoing a laparoscopic procedure for resection of stage I-IV endometriosis, hysterectomy, myomectomy, salpingectomy, oophorectomy, cystectomy, urethropexy, adhesiolysis or any combination of these surgeries who would possibly require post-operative drainage were approached for inclusion in the study; female aged 18-80; fluent in spoken and written English, able to understand implications of their involvement in the study and those who consent to involvement in the study.
排除标准
- •Exclusion criteria include patients who may become distressed due to involvement in the study, intercurrent conditions precluding participation, known or suspected pregnancy and known or suspected gynecological malignancy. Women who have not been previously sexually active will be excluded from transvaginal ultrasound assessment
研究者
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