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GRIP: Gordian Robotic Integrated Port Closure Study

NCT07649915 · Gordian Surgical · Updated 16 June 2026

What is being tested
Fascial closure device
For
Robotic Surgery
Kind of study
Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
Who can join
Ages 18 years to 95 years. About 26 people. The full rules are on the registry page.
Where
United States
When
Starts or started 30 June 2026, ends 30 Dec 2026. Registered 16 June 2026.
Results
None posted yet.

In the researchers' words

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.
ClinicalTrials.gov, NCT07649915

Sites

  • AHN Allegheny General HospitalPittsburgh, Pennsylvania, United States