About this trial
This study aims to determine whether Ropivacaine-Poloxamer 407 hydrogel provides non-inferior pain control compared to TAP block for patients undergoing minimally invasive gastrectomy. The results will guide postoperative pain management practices and enhance recovery protocols for gastric cancer surgery.
Eligibility criteria
Qualifiers
Patients with a histologically confirmed diagnosis of gastric adenocarcinoma prior to surgery.
Patients who have undergone a complete surgical resection (R0 resection).
Patients with an ASA (American Society of Anesthesiologists) score of 3 or below.
Patients aged 20 years or older.
Disqualifiers
Patients under 19 years of age.
Presence of ascites or peritoneal metastasis.
Patients who have undergone preoperative chemotherapy or radiotherapy.
Diagnosis of malignancies other than gastric cancer.
Trial design
Treatments tested in this trial
- Arm I (Ropivacaine-Poloxamer 407 hydrogel group)
- Arm II (TAP block group)