A stitch in time: could a device make abdominal closure safer?

NCT ID NCT07766044

First seen Aug 14, 2026 · Last updated Aug 14, 2026

Summary

This trial compares two ways of closing the abdomen after open colorectal surgery: a device-assisted method (SutureTOOL) versus the traditional manual technique. The goal is to see if the device helps reduce the chance of an incisional hernia forming within one year. Participants are adults undergoing elective surgery through a midline incision for colorectal disease. The study also tracks short-term issues like wound infections and wound separation.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance
A device-assisted closure technique using the SutureTOOL device versus manual closure with standard needle driver and curved needle.
What this could lead to
If successful, this could point toward a standardized closure method that reduces incisional hernias and other abdominal wall complications after open colorectal surgery.
What could go wrong
This is a single study with a limited number of participants, and results may not apply to all patients. The device may not significantly reduce hernia rates compared to careful manual closure.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for COLORECTAL CANCER are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Conditions

The condition(s) this trial relates to.

colorectal cancer colorectal neoplasm Incisional Hernia Wound Infection

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Helsingborg hospital

    RECRUITING

    Helsingborg, Skåne County, 251 87, Sweden

More trials for these conditions

Other studies related to the condition(s) this trial covers.