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临床试验/NCT03373513
NCT03373513撤回不适用

Robotic-assisted Hysterectomy: Single- vs. Multi-port Laparoscopic Access

Herning Hospital2 个研究点 分布在 1 个国家目标入组 124 人开始时间: 2019年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
发起方
入组人数
124
试验地点
2
主要终点
Return-to-work

研究概览

简要总结

robotic single site surgery (R-SSH) is a novel technique, which may be superior to conventional multiport hysterectomy in select patients regarding cosmesis and postoperative pain. We, perform a randomized trial to compare R-SSH with multiport laparoscopic hysterectomy with regard to the postoperative rehabilitation, cosmesis, the operational cost, and the perioperative morbidity.

详细描述

The study is scheduled to start February 2018 and compares robotic single-site hysterectomy to conventional multiport hysterectomy. Procedures are performed by an experienced two-surgeon team. Patients are randomized to either conventional multiport hysterectomy (N=62) or R-SSH (N=62). Eligibility criteria are the same as for study 1. Patient's satisfaction with body image and cosmesis is assessed at different time points pre- and postoperatively by means of validated cosmesis scales and Body Image Questionnaire. Postoperative pain and analgesia use will be registered as well as secondary outcome parameters as described above. A follow-up at 1, 3 and 6 month include evaluation of the scar and registration of port-site hernias and vaginal dehiscence or other complications. Interviews and diaries will include time of return to home and work, daily activities including sexuality The R-SSH is performed using da Vinci, Xi robotic system. One single port, diameter 2 cm is applied. Applying an additional assistant port is defined conversion of procedure The laparoscopy is performed using our standard equipment and 4 trocars, 5 mm each.

Socio-economical consequences of R-SSH versus conventional laparoscopic hysterectomy Study details in preparation

Sample size calculation was based a previous study on fast track hysterectomy, which showed a difference in return to work of 4 days. 62 women in each group is needed with standard deviation ±8 and a power of 80%. To include those not working, we calculated that with an expected visual analog pain score of 0.86 ±0.2 and 62 in each group the sample was sufficient to detect of difference of 0.1 in visual analog pain score with a power of 80%. All calculation are based on two-sided testing with alpha of 0.05.

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
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • hysterectomy on benign indication,
  • American Society of Anesthetists group 1 or 2,
  • BMI less than 35 kg/m2
  • uterine size less than 300 g estimated by ultrasound, using Ferraris formula.

排除标准

  • adhesions
  • prior extensive abdominal surgery
  • prior midline incision,
  • cutis laxa of abdomen surgery
  • endometriosis
  • more than 1 cesarean section
  • malignant disease

研究组 & 干预措施

Robotic single-site hysterectomy

Active Comparator

Robotic single-site hysterectomy is performed in this arm

干预措施: Robotic single-site Hysterectomy (Procedure)

Multiport Laparoscopy

Active Comparator

Multiport Laparoscopic hysterectomy is performed in this other arm

干预措施: Laparoscopic hysterectomy (Procedure)

结局指标

主要结局

Return-to-work

时间窗: up to six months after operation or until work is resumed, whichever came first

Time from operation to return work

次要结局

  • Pain measured by subjective score(Visual analogue pain score first, second, third, fourth, fifth, and six months after operation)

研究者

发起方
Herning Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Finn Lauszus

Research Specialist, Senoir Consultant, Assistant Professor

Herning Hospital

研究点 (2)

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