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Study on a novel laparoscopic trocar with built-in fascial closure function (CLOCAR)

Prospective study on the safety and efficacy of a novel laparoscopic trocar with built-in fascial closure function (CLOCAR)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0003389
Enrollment
55
Registered
2018-12-13
Start date
2019-03-05
Completion date
Unknown
Last updated
2022-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

The Catholic University of Korea, St. Vincent's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who used laparoscopic ports over 10mm during laparoscopic or robotic surgery 2) aged over 18, under 80 3) Patients who voluntarily agreed in writing to participate in the trial

Exclusion criteria

Exclusion criteria: 1) Patients who underwent simultaneous operations other than laparoscopic/robotic surgery 2) Patients with severe head injury or stroke or a history of the disease 3) Patients living in a nursing home or accommodation with poor cognitive ability 4) Patients with acute or chronic medical or psychiatric conditions or laboratory abnormalities that are not appropriate for participation in the clinical study 5) Patients who are judged to be unappropriate for the clinical study

Design outcomes

Primary

MeasureTime frame
Time for port-site closure—

Secondary

MeasureTime frame
Port-site hernia;Port-site infection;Port-site ascitic leak;Injury to adjacent organs;Gas leak;Need for additional instrument;Durability—

Countries

Korea, Republic of

Contacts

Public ContactHee Youn Kim

The Catholic University of Korea, St. Vincent's Hospital

khyoun10589@gmail.com+82-31-249-8748

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026