Stomach Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been confirmed by laboratory testing to have a type of stomach cancer called gastric adenocarcinoma before surgery
- People who have had surgery that completely removed the cancer with no cancer cells left at the edges (a complete removal)
- People who have been given an anaesthesia risk score of 3 or lower by their medical team, indicating they are considered suitable for surgery
- People aged 20 years or older
- People who had their stomach surgery performed using laparoscopic (keyhole) or robotic techniques
Who may not be able to join:
- People under 19 years of age
- People who have fluid build-up in the abdomen or cancer that has spread to the lining of the abdomen
- People who received chemotherapy or radiation treatment before their surgery
- People who have been diagnosed with a cancer other than stomach cancer
- People with uncontrolled diabetes, autoimmune conditions, or a history of abnormal scarring (such as raised or thickened scars) that could affect wound healing
- People with a known allergy or past bad reaction to the local anaesthetic Ropivacaine or similar local anaesthetic medicines
- People who are pregnant
- People who had long-term pain conditions before surgery, including a condition called Complex Regional Pain Syndrome (CRPS) (confirm with trial site)
- People who were regularly using strong opioid pain medicines before their surgery
- People with mental health conditions that the medical team believes would make it difficult to take part in the study
- People with serious liver disease, serious kidney disease, or heart rhythm problems
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 82-2-2019-4601
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Total fentanyl consumption within 72 hours postoperatively.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.