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Effects of general anesthesia combined with TEA and general anesthesia on short-term clinical outcomes after laparoscopic gastric cancer surgery in elderly patients: a single-center randomized controlled study

Effects of general anesthesia combined with TEA and general anesthesia on short-term clinical outcomes after laparoscopic gastric cancer surgery in elderly patients: a single-center randomized controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020215
Enrollment
Unknown
Registered
2018-12-20
Start date
2018-12-25
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

gastric cancer

Interventions

Group 1:Use general anesthesia combined with epidural anesthesia
Group 2:Use general anesthesia

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients aged between 65 and 75 who have not received preoperative neoadjuvant therapy and who are planning to undergo laparoscopic radical gastrectomy

Exclusion criteria

Exclusion criteria: 1. Participating in another concurrent intervention trial; 2. American Society of Anesthesiologists (ASA) Physical Status Score of V; 3. Any contraindication for epidural anesthesia; 4. Patients with allergy to the study drugs; 5. Previous extensive abdominal surgery (any open or laparoscopic abdominal surgery except laparoscopic appendectomy, cholecystectomy, or hernia repair); 6. Cardiac insufficiency more than III grade (NYHA); 7. Intake of opioid analgesics, or steroids > 5 mg/day for = 7 days before surgery; 8. Long term history of intake of glucocorticoid and gastrointestinal motility drugs; 9. Under anti-depressive medication; 10. Patient with primary diabetes and impaired glucose tolerance, hyperthyroidism and hypothyroidism; 11. Severe obesity (BMI > 32) and severe malnutrition (BMI < 15); 12. History of constipation; 13. Pregnancy, lactation, or childbearing potential without using adequate contraception.

Design outcomes

Primary

MeasureTime frame
gastrointestinal function recovery;

Secondary

MeasureTime frame
occurrence of postoperative complications;postoperative hospital stays;visual analog pain scales (VAS);inflammatory factors;biochemical parameters;Arterial Blood Gas Analysis;Narcotic dosage;

Countries

China

Contacts

Public ContactJian Zhang

Affiliated Hospital of Qingdao University

drjianzhang@126.com+86 18661801310

Outcome results

None listed

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