跳至主要内容
临床试验/NCT07649915
NCT07649915尚未招募不适用

Gordian Robotic Integrated Port Closure Using the TroClose™ 1200 With the da Vinci® 12 mm Robotic Assistant Port

Gordian Surgical1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2026年6月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
26
试验地点
1
主要终点
Technical Success; To determine the ability of the TroClose™ 1200 to achieve fascial closure when used with a 12mm da Vinci® robotic assistant port during robotic surgery

研究概览

简要总结

The GRIP (Gordian Robotic Integrated Port Closure) Study is a prospective, single-arm feasibility study evaluating the use of the TroClose™ 1200 device for closure of da Vinci® 12 mm robotic assistant port sites following robotic-assisted surgical procedures.

TroClose™ 1200 is an FDA-cleared medical device designed to facilitate fascial closure of laparoscopic and robotic access ports. The device deploys anchors and suture at the beginning of the procedure, allowing closure to be completed at the end of surgery without the need for additional needle passage or specialized closure instruments.

The purpose of this study is to assess the safety, feasibility, procedural performance, and clinical outcomes associated with use of the device in patients undergoing robotic-assisted surgery. Study assessments will include successful port-site closure, device-related adverse events, post-operative complications, and short-term follow-up evaluations.

Approximately 26 adult participants undergoing robotic-assisted surgical procedures at Allegheny Health Network will be enrolled.

详细描述

GRIP (Gordian Robotic Integrated Port Closure) is a prospective feasibility study evaluating the use of the TroClose™ 1200 device for closure of da Vinci® 12 mm robotic assistant port sites following robotic-assisted surgical procedures.

TroClose™ 1200 is an FDA-cleared Class II medical device designed to facilitate fascial closure of laparoscopic and robotic access ports. The device deploys fixation anchors and suture during port insertion, allowing closure of the fascial defect at the completion of the procedure without the need for additional needle passage through the abdominal wall. This approach is intended to provide a standardized and reproducible closure technique while minimizing additional procedural steps at the conclusion of surgery.

Robotic surgery continues to expand across multiple surgical specialties, resulting in increased utilization of 12 mm robotic assistant ports. Appropriate closure of fascial defects associated with larger trocar sites remains an important consideration for reducing port-site complications and maintaining procedural efficiency. The GRIP study is designed to evaluate the performance of a pre-positioned closure system within the robotic surgical environment.

Participants undergoing eligible robotic-assisted surgical procedures will receive closure of a designated da Vinci® 12 mm assistant port using the TroClose™ 1200 device according to the study protocol. The study will assess device utilization within routine clinical practice and characterize procedural performance, workflow integration, and safety outcomes associated with use of the device in robotic-assisted surgery.

Data generated through this investigation will contribute to the understanding of pre-positioned fascial closure techniques for robotic surgery and may inform future clinical studies, publications, and broader adoption of robotic port-site closure technologies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males or female patients age 18 to 95 years old
  • Scheduled to undergo an elective, clinically indicated robotic surgery with a da Vinci® 12 mm assistant port
  • Trocar site is appropriate for TroClose™ per Investigator/Surgeon discretion
  • Subject is able and willing to sign a written informed consent form

排除标准

  • Scheduled to undergo emergency surgery
  • Weight under 45kg (99.2 pounds)
  • Infection at port site
  • Prior surgical mesh at intended incision location
  • Surgeon-determined contraindication for use of the TroClose™ 1200
  • Inability to provide written, informed consent
  • Known allergy to PGA (Polyglycolic Acid)
  • PLA (Polylactic Acid).

研究组 & 干预措施

Interventional - TroClose1200 with DaVinci Robot

Experimental

This intervention will assess affective fascial closure utilizing the TroClose1200 device in DaVinci Robotic procedures.

干预措施: Fascial closure device (Device)

结局指标

主要结局

Technical Success; To determine the ability of the TroClose™ 1200 to achieve fascial closure when used with a 12mm da Vinci® robotic assistant port during robotic surgery

时间窗: 30 days

Measured by confirmation of fascial closure by digital (finger) palpation - Measured as either closed or not closed.

次要结局

  • Safety; Freedom from peri operative serious adverse events(30 days)

研究者

发起方
Gordian Surgical
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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