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Clinical Cohort Study on the Acceleration of Postoperative Recovery in Patients Undergoing Open Radical Gastrectomy with Multimodal Postoperative Management Based on Continuous Incisional Analgesia

Clinical Cohort Study on the Acceleration of Postoperative Recovery in Patients Undergoing Open Radical Gastrectomy with Multimodal Postoperative Management Based on Continuous Incisional Analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117088
Enrollment
Unknown
Registered
2026-01-20
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative recovery of gastric cancer

Interventions

Control group:None

Sponsors

Ningbo Medical Centre Lihuili Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-80 years old; 2.Underwent elective radical gastrectomy for gastric cancer (total gastrectomy or distal gastrectomy) at our hospital during the specified study period; 3.Treatment group: Clearly documented to have undergone open surgery, with postoperative management adopting "multimodal postoperative management based on continuous incisional analgesia" (i.e., the medical records clearly document the placement of a continuous incisional analgesia catheter/pump, combined with at least one other non-opioid or mechanistically distinct analgesic drug/method); 4.Control group: Clearly documented to have undergone laparoscopic surgery, with postoperative management adopting conventional analgesia regimens (such as patient-controlled intravenous analgesia alone, or as-needed oral/intramuscular analgesic medications, without the use of continuous incisional analgesia techniques); 5.Key perioperative data (such as pain scores, complication records, admission/discharge times, etc.) are fully documented in the medical records.

Exclusion criteria

Exclusion criteria: 1.Patients undergoing emergency surgery, palliative surgery, or combined multi-organ resection; 2.Patients with a history of chronic pain or long-term regular use of opioid or potent analgesic medications; 3.Patients with severe psychiatric or neurological disorders who are unable to cooperate or accurately report pain; 4.Patients allergic to local anesthetics (e.g., ropivacaine) (primarily for screening the treatment group); 5.Patients transferred to the ICU for non-rehabilitation reasons for more than 24 hours postoperatively; 6.Patients with severely incomplete clinical medical records, making it impossible to evaluate primary or secondary outcome measures.

Design outcomes

Primary

MeasureTime frame
Intensity of pain;

Secondary

MeasureTime frame
Hospitalization period;Gastrointestinal function recovered;Eat by mouth;Early Activities;Utilization of medical resources;Hospitalization expenses;Pain relief-related indicators;The occurrence of complications;

Countries

China

Contacts

Public ContactXianlei Cai

Ningbo Medical Centre Lihuili Hospital

xianleicai@163.com+86 574 55836135

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026