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Application of accelerated rehabilitation surgery in elderly patients with gastric cancer

Application of accelerated rehabilitation surgery in elderly patients with gastric cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068532
Enrollment
Unknown
Registered
2023-02-22
Start date
2023-03-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Gastric cancer in the elderly

Interventions

Experimental group:Accelerated rehabilitation program for elderly gastric cancer

Sponsors

Affiliated Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years old; 2. Have not received anti-tumor treatment such as chemotherapy before operation; 3. All received elective D2 surgical treatment; 4. Informed consent of patients and their families.

Exclusion criteria

Exclusion criteria: 1. Those who are deemed unsuitable to participate in this experiment by the doctor; 2. Patients with gastric cancer aged II class (NYHA), patients who recently underwent coronary artery bypass grafting (CABG), patients with severe hypertension (systolic blood pressure >= 180 mmHg or diastolic blood pressure >= 110 mmHg); 4. Patients with severe infection, respiratory insufficiency, coagulation dysfunction, severe liver and renal insufficiency and other severe organ dysfunction (Child-Pugh >= 10 points; creatinine clearance rate 10% or SGA nutritional status evaluation grade C, BMI < 18, Hb < 70 g/L); 9. Patients who cannot complete the accelerated recovery surgery procedure or have obvious contraindications for accelerated recovery surgery; 10. Patients with severe edema, infection, and peripheral blood circulation disorders; 11. Pregnant and lactating women, subjects (including male subjects) who have pregnancy plans within one month after the test; 12. Participate in other clinical trials within 3 months before the trial; 13. Sponsors or investigators directly involved in the trial or their family members; 14. The patient or the patient's family members do not agree to participate in fast recovery surgery.

Design outcomes

Primary

MeasureTime frame
Number of days of preoperative and postoperative hospital stay;

Secondary

MeasureTime frame
Indicator of gastrointestinal function recovery;Nutritional and physical status indicators;The number of days that the abdominal drainage tube is indwelled;Indicators of stress and inflammation;Intestinal microecology;Heart rate variability;Postoperative activity;Postoperative complications;The total cost of treatment;Patient and family satisfaction;Immune indicators;Operation;Tumor condition;Postoperative pain score;Nutritional indexes;

Countries

China

Contacts

Public ContactChen Jixiang

Affiliated Hospital of Jiangsu University

cyok9@163.com+86 137 7555 2338

Outcome results

None listed

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