Plain-English translation of NCT07676370 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Ovarian Cancer research guide →This study doesn't follow the usual testing phases — it may be an observational study or a different type of research.
This trial is testing whether placing a special mesh during ovarian cancer surgery can prevent a common complication called incisional hernia—when the surgical wound weakens and bulges over time. Women with ovarian cancer who need abdominal surgery will be randomly assigned to receive either the mesh reinforcement or standard closure, and some will also receive special wound therapy after surgery to see which approach works best.
After major abdominal surgery for ovarian cancer, many patients develop weak spots or bulges at their surgical incision that can cause pain, limit activities, and require additional surgery. Researchers want to see if adding mesh during the initial surgery can prevent this problem from happening in the first place.
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You will undergo your planned ovarian cancer surgery, and during the procedure your surgeon will randomly assign you to one of four groups: mesh with or without special wound therapy, or standard closure with or without special wound therapy. After surgery, you will follow your assigned treatment plan and return for follow-up visits over the next 24 months so researchers can monitor whether your incision heals properly and whether you develop any complications.
AI-generated summary from trial data · Jul 18, 2026 · Not medical advice
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