Preventing Hernia After Gastrointestinal Surgery

This study is looking at whether a special type of stitch called Stratafix Symmetric™ can help prevent incisional hernias (a bulge that can form near a surgical cut) after major gastrointestinal or abdominal surgery. Researchers will compare Stratafix Symmetric™ to the standard stitches currently used. You might be able to join if you are 18 or older, a patient at West Michigan Cancer Center, and having certain liver, pancreas, biliary, or gastrointestinal surgery, or other major cancer surgery. The main goal is to see how many people develop a hernia within 12 months. The study also aims to check the safety of Stratafix Symmetric™ and its effect on your pain and quality of life. The current recruitment status is unclear.

Study design
This interventional study plans to enroll 100 participants. It compares two different types of sutures.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed from enrollment until the end of study participation at 12 months.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06063577

Use of Stratafix Symmetric™ to Prevent Incisional Hernia in Gastrointestinal and Abdominal Surgery

Recruiting
NAAges 18+InterventionalTreatment
West Michigan Cancer Center
~100 participants
Updated 2024-02-02 on ClinicalTrials.gov
What's tested:Stratafix sutureStandard of care suture

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Number of participants who develop ventral incisional hernia
Measured over From enrollment to end of study participation at 12 months
C.Surgical Procedure; Disruption of Wound, Suture
1 sites across 1 states
Michigan1
  • Gitonga Munene · PRINCIPAL_INVESTIGATOR · West Michigan Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

  • Number of participants who develop ventral incisional herniaFrom enrollment to end of study participation at 12 months

    Infection, seroma, surgical site infection, evisceration, mesh rejection, systemic complications