A Prospective study, using the VersaOne Fascial Closure system during abdominal wall closure at port insertion site in laparoscopic surgery

A Prospective study, using the VersaOne Fascial Closure system during abdominal wall closure at port insertion site in laparoscopic surgery - A Prospective study, using the VersaOne Fascial Closure system during abdominal wall closure at port insertion site in laparoscopic surgery

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000041336

Enrollment

200

Registered

2020-08-07

Start date

2020-08-07

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

gastrointestinal disease

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1)Cases using a 12 mm port in cases undergoing laparoscopic surgery 2)A case in which the thickness from the skin to the peritoneum measured by CT is 30 mm or more at the planned port insertion site 3)Latest test results within 2 months prior to registration, maintaining organ function required for surgery under general anesthesia 4)Written consent has been obtained from the study participant 5)Excludes patients with a history of open surgery and previous wounds at the site of planned port insertion 6) Other cases considered inappropriate by the attending physician are excluded.

Exclusion criteria

Exclusion criteria: Patients with a history of previous laparotomy and a history of injury at the site where the port is to be inserted or other complications or treatment courses that the attending physician deems inappropriate

Design outcomes

Primary

Measure	Time frame
Fascial closure time of 12mm port	—

Countries

Japan

Contacts

Public ContactMasayuki Ishii

Sapporo Medical University Hospital Department of Surgery, Surgical Oncology and Science

masayuki-ishii@sapmed.ac.jp0116112111

Outcome results