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 through laboratory testing to have a type of stomach cancer called gastric adenocarcinoma, before having surgery.
- People who have had surgery that successfully removed all of the cancer with clear margins (known as a complete or R0 resection).
- People whose overall health before surgery was rated at a certain level of fitness for anaesthesia (an ASA score of 3 or below — confirm with trial site if unsure what this means).
- People aged 20 years or older.
Who may not be able to join:
- People who are 19 years of age or younger.
- People who have fluid build-up in the abdomen (ascites) or cancer that has spread to the lining of the abdomen (peritoneal metastasis).
- People who received chemotherapy or radiotherapy before their surgery.
- People who have been diagnosed with a cancer other than stomach cancer.
- People with uncontrolled diabetes, autoimmune diseases, or a history of abnormal scarring (such as hypertrophic scars or keloids) that could affect wound healing.
- People who have had an allergic reaction or other adverse reaction to Ropivacaine or any other local anaesthetic medicines.
- People who are pregnant.
- People who had ongoing (chronic) pain conditions before surgery, including a condition called Complex Regional Pain Syndrome (CRPS).
- People who were using opioid pain medicines regularly over a long period before surgery.
- People with a psychiatric condition that is considered likely to interfere with taking part in the study.
- People with severe liver disease, severe kidney disease, or irregular heart rhythms (arrhythmia).
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: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.