Clinical trial · Interventional
The Safe Study of Routine Closure of Mesenteric Defects Versus Non-closure After Radical Gastrectomy
A Multicenter, Randomized, Controlled Clinical Trial of the Safety of Mesenteric Defects Closure After Radical Gastrectomy
NCT05356156CI-TRIAL-00058183not yet recruitingN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To compare the incidence of internal hernia, overall survival and short-term surgical safety of routine closure of the surgically created mesenteric defects versus non-closure for patients with adenocarcinoma of the gastric or esophagogastric junction who underwent radical gastrectomy (D1+/D2 lymph node dissection).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Closure of the mesenteric defects | Procedure | — | UNRESOLVED |
| Non-closure of the mesenteric defects | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Closure of the mesenteric defects
- description
- Closure of the mesenteric defects will be performed after radical gastrectomy in patients with gastric or esophagogastric junction adenocarcinoma.
- interventionNames
- Procedure: Closure of the mesenteric defects
- type
- ACTIVE_COMPARATOR
- label
- Non-closure of the mesenteric defects
- description
- Non-closure of the mesenteric defects will be performed after radical gastrectomy in patients with gastric or esophagogastric junction adenocarcinoma.
- interventionNames
- Procedure: Non-closure of the mesenteric defects
Primary outcomes (1)
- measure
- The incidence of internal hernia within 3 years after surgery
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Aged 18-75 years; * Primary lesion is diagnosed with endometrial biopsy as adenocarcinoma of the stomach or esophagogastric junction, including: papillary adenocarcinoma, tubular adenocarcinoma, mucinous adenocarcinoma, poorly cohesive carcinoma (including signet ring cell carcinoma and other variants), mixed adenocarcinoma, etc.; * The gastric primary lesion is located in the antrum, body or fundus of stomach or the esophagogastric junction. It is expected that radical gastrectomy with D1+/D2 lymph node dissection achieves R0 resection (multiple primary cancers are also applicable); * BMI(Body Mass Index) \< 30 kg/m2; * No history of upper abdominal surgery (except for laparoscopic cholecystectomy); * No prior treatment of chemotherapy, radiotherapy, targeted therapy, immunotherapy, etc.; * Preoperative ECOG (Eastern Cooperative Oncology Group) performance status score 0 or 1; * Preoperative ASA (American Society of Anesthesiologists) scoring I-III; * Sufficient vital organ functions; * Signed informed consent. Exclusion Criteria: * Women during pregnancy or lactation; * Suffer from other malignant tumors within 5 years; * Preoperative body temperature ≥ 38°C or complicated with infectious diseases requiring systemic treatment; * Severe mental illness; * Severe respiratory disease; * Severe liver and kidney dysfunction; * History of unstable angina or myocardial infarction within 6 months; * History of cerebral infarction or cerebral hemorrhage within 6 months; * Continuous application of glucocorticoid within 1 month (except for topical application); * Accompanied by gastric cancer complications (bleeding, perforation, obstruction, etc.) ; * The patient has participated in or is participating in other clinical studies (within 6 months).
References
Publications (0)
Data not yet available
No reference posted for this study.