Safety of Opportunistic Salpingectomy During Elective Laparoscopic Cholecystectomy.
Safety of Opportunistic Salpingectomy During Elective Laparoscopic Cholecystectomy: A Randomized Controlled Trial
The knowledge, coupled with epidemiological studies demonstrating lower ovarian cancer rates in women with a history of tubal sterilization has led to recommendations for opportunistic salpingectomy at the time of benign gynecological surgery. However, this recommendation was not explored in the setting of non-gynecological surgeries, of most if the surgery performed not in pelvis.
This study aims to evaluate the safety of performing opportunistic salpingectomy at the time of elective laparoscopic cholecystectomy in women aged 45 years or older. Of note, the only available prospective study from Austria evaluated feasibility of combined operation. By assessing complication rates and other perioperative outcomes, the study seeks to determine if this combined approach is a safe for opportunistic ovarian cancer prevention. Ultimately, this research may inform surgical practice and potentially reduce the incidence of ovarian cancer in this population.
研究概览
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Zurich、瑞士、8091
- Division of Visceral Surgery and Transplantation , University Hospital Zurich
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Women aged 45 years or older.
- No known history of ovarian or fallopian tube cancer.
- Completed family planning.
- Scheduled to undergo elective laparoscopic cholecystectomy for benign gallbladder disease.
- Able to provide informed consent.
- Willing to comply with study procedures and follow-up assessments.
Exclusion Criteria:
- Previous abdominal Surgery or any inflammatory bowel disease.
- Current pregnancy or breastfeeding (verbally asked).
- Contraindications to laparoscopic surgery (e.g., severe cardiopulmonary disease, extensive prior abdominal surgery).
- Any medical condition that, in the opinion of the investigator, would preclude safe participation in the study or interfere with follow-up.
- Participation in another clinical trial that may confound the results of this study.
学习计划
研究是如何设计的？
设计细节
- 主要用途：预防
- 分配：随机化
- 介入模型：并行分配
- 屏蔽：无（打开标签）
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的：Experimental group
Opportunistic salpingectomy during surgery.
|
Opportunistic salpingectomy at the time of elective laparoscopic cholecystectomy will be performed in study group, while the control group undergo cholecystectomy without salpingectomy.
Cholezystectomy as controll group
|
|
有源比较器：Control group
Elective cholecystectomy
|
Cholezystectomy as controll group
|
研究衡量的是什么？
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Postoperative complications assesed with Comprehensive complication index.
大体时间：within 6 weeks after surgery
|
This will be the primary outcome measure, encompassing any complications assessed with Comprehensive Complication Index.
The range between 0 and 100.
The higher score means more complications.
|
within 6 weeks after surgery
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Operating time
大体时间：Operating time in minutes during surgical procedure
|
Operating time measured in minutes from incision until skin stich
|
Operating time in minutes during surgical procedure
|
|
Length of hospital stay
大体时间：Length of hospital stay: The number of days patients remain hospitalized after surgery untill discharge assedd at discharge (assessed at around 5 days).
|
Length of hospital stay calculated in days
|
Length of hospital stay: The number of days patients remain hospitalized after surgery untill discharge assedd at discharge (assessed at around 5 days).
|
合作者和调查者
调查人员
- 首席研究员：Dilmurodjon MDE Eshmuminov, MD、Univercity hospital zurich
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.