跳至主要内容
临床试验/NCT07313839
NCT07313839招募中不适用

Comparison Between Double-Layer Self-Locking and Traditional Sutures in Post-Hysterectomy Laparoscopic Colporrhaphy: A Multicenter Pragmatic Randomized Controlled Trial

Azienda Ospedaliero-Universitaria di Parma6 个研究点 分布在 1 个国家目标入组 310 人开始时间: 2025年10月7日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
310
试验地点
6
主要终点
Vaginal cuff dehiscence rate

研究概览

简要总结

Vaginal vault closure after laparoscopic or robotic hysterectomy may be associated with postoperative complications such as vaginal cuff dehiscence, infection, and bleeding. The optimal suture material and technique for laparoscopic colporrhaphy, particularly in patients undergoing surgery for gynecologic malignancies, remain controversial.

The BI-SURE trial is a multicenter, randomized controlled study designed to compare double-layer self-locking sutures versus double-layer traditional Polyglactin 910 sutures for laparoscopic vaginal vault closure after hysterectomy. The study aims to evaluate postoperative effectiveness and safety within three months after surgery.

详细描述

Laparoscopic and robotic hysterectomy represent standard surgical approaches for the treatment of gynecologic malignancies but are associated with a higher risk of vaginal vault complications compared with open or vaginal surgery. Although uncommon, postoperative complications such as vaginal cuff dehiscence, infection, and bleeding may lead to significant morbidity and require additional medical or surgical interventions.

Vaginal vault closure can be performed using different suturing techniques and materials. Traditional braided sutures, such as Polyglactin 910, are widely used in clinical practice, while self-locking (barbed) sutures have been introduced to facilitate laparoscopic suturing by maintaining tissue approximation without the need for knots. Evidence comparing these sutures is limited, particularly for double-layer closure techniques and in patients treated for gynecologic malignancies.

The BI-SURE trial is a multicenter, pragmatic, randomized controlled trial designed to compare double-layer self-locking sutures versus double-layer traditional Polyglactin 910 sutures for laparoscopic vaginal vault closure following hysterectomy for malignant gynecologic disease. Eligible patients will be randomized in a 1:1 ratio. Postoperative outcomes will be assessed up to three months after surgery, including vaginal cuff-related complications and postoperative pain.

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
Triple (Participant, Investigator, Outcomes Assessor)

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

  • Patients undergoing laparoscopic or robotically assisted hysterectomy for gynecologic malignant disease
  • Age ≥ 18 years
  • Ability to provide written informed consent

排除标准

  • Laparotomic or vaginal hysterectomy
  • Contraindication to laparoscopic vaginal vault closure

研究组 & 干预措施

Self-Locking Suture Group

Experimental

Participants randomized to this arm will undergo laparoscopic vaginal vault closure after hysterectomy using a double-layer continuous suturing technique performed with a self-locking (barbed) suture, according to current clinical practice.

干预措施: Double-Layer Vaginal Vault Closure with Self-Locking Suture (Procedure)

Traditional Suture Group

Active Comparator

Participants randomized to this arm will undergo laparoscopic vaginal vault closure after hysterectomy using a double-layer continuous suturing technique performed with traditional braided Polyglactin 910 suture, according to current clinical practice.

干预措施: Double-Layer Vaginal Vault Closure with Polyglactin 910 (Procedure)

结局指标

主要结局

Vaginal cuff dehiscence rate

时间窗: Within 3 months after surgery

Proportion of participants experiencing vaginal cuff dehiscence requiring surgical reintervention after laparoscopic hysterectomy.

Vaginal cuff infection rate

时间窗: Within 3 months after surgery

Proportion of participants developing vaginal cuff infection, defined as abnormal vaginal discharge with or without fever, leukocytosis, and/or local tenderness, requiring antibiotic therapy.

Postoperative bleeding rate

时间窗: Within 3 months after surgery

Proportion of participants experiencing postoperative vaginal cuff bleeding requiring hemostatic treatment.

次要结局

  • Postoperative pain intensity(At 1 month and 3 months after surgery)
  • Early postoperative composite complication rate(Within 1 month after surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Vito Andrea Capozzi

Principal Investigator

Azienda Ospedaliero-Universitaria di Parma

研究点 (6)

Loading locations...

相似试验