Clin2
NCT06255314Possibly a fitNot yet recruiting

Minimally invasive surgery for ventral hernia repair

Ventral Hernia

Part of Digestive system clinical trials.

This study compares minimally invasive (laparoscopic) techniques for repairing ventral hernias, which are bulges in the belly area. The goal is to see which method leads to better outcomes, such as less pain and faster recovery.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
45 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must be 18 years or older and able to give your informed consent (agree to participate after understanding the study).
  • You must have a ventral hernia—this includes umbilical (belly button), paraumbilical (near belly button), epigastric (upper belly), spigelian (side of belly), or incisional (after a previous surgery) hernias.
  • You cannot have an inguinal hernia (groin hernia).
  • You cannot have a strangulated or obstructed hernia (a hernia that is trapped or blocking the intestine, an emergency).
  • You cannot have had a previous hernia repair with a mesh.
  • Your hernia defect (the hole in the muscle) must be no larger than 10 cm.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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