Primary Mesh Closure of Abdominal Midline Wounds A double blind Randomized Controlled Trial

Primary Mesh Closure of Abdominal Midline Wounds A double blind Randomized Controlled Trial - PRIMA trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON39427

Enrollment

280

Registered

2007-10-01

Start date

2009-02-03

Completion date

Unknown

Last updated

2024-06-18

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

Conditions

ventrale hernias na laparotomie (chirurgische complicatie) incisional hernia

Interventions

During the closure of the abdomen a mesh will be placed on or in the abdominal wall.

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Every elective midline laparotomy for patients with Abdominal Aortic Aneurysm and patients with a BMI of more than 27.

Exclusion criteria

Exclusion criteria: · Age

Design outcomes

Primary

Measure	Time frame
Primary outcome · Incisional hernia occurrence	—

Secondary

Measure	Time frame
Secondary outcome · Postoperative complications · Pain · Quality of life · Cost effectiveness	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)