The Effect of Vertical Versus Horizontal Vaginal Cuff Closure on Vaginal Length After Laparoscopic Hysterectomy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 43
- 试验地点
- 2
- 主要终点
- Vaginal length
研究概览
简要总结
This study has been designed as a prospective randomized trial to be performed at Bridgeport Hospital. Patients planning to undergo a laparoscopic or robotically assisted total laparoscopic hysterectomy with or without removal of adnexal structures will be recruited by the Bridgeport Hospital Minimally Invasive Gynecologic Surgery fellows during their preoperative office visit at the Bridgeport Hospital Gynecologic Oncology office. If enrolled, they will be assigned a sequential study identification number. During their preoperative exam, a baseline POP-Q will be performed. Demographic information will be recorded from the electronic medical record.
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
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Undergoing laparoscopic or robotic-assisted laparoscopic hysterectomy
- •Under the care of Dr. Dan-Arin Silasi or Dr. Masoud Azodi at Bridgeport Hospital
- •Planning to follow up at the Gynecologic Oncology office at Bridgeport Hospital
- •Age 18 or older
- •Able to give informed consent to participate in the research study
排除标准
- •Age less than 18
- •Unable to give informed consent
- •Patients undergoing radical hysterectomy
- •Patients receiving vaginal cuff radiation within the study period
- •Patients undergoing concomitant pelvic floor or vaginal suspension procedure
结局指标
主要结局
Vaginal length
时间窗: 1-3 weeks postop
Vaginal length will be measured in cm by standard POP-Q measurements
次要结局
- Vaginal length(3-4 months postop)
- Cuff closure time(intra-op)