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The clinical trial of opioid-sparing anesthesia undergoing major laparoscopic abdominal surgery

The clinical trial of opioid-sparing anesthesia undergoing major laparoscopic abdominal surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060130
Enrollment
Unknown
Registered
2022-05-19
Start date
2022-05-06
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Pancreatic tumors, liver tumors, stomach and intestinal tumors

Interventions

Remifentanil group:Remifentanil continuous infused with 0.2-0.5ug/kg/h
Low-opioid anesthesia group:Esketamine and dexmedetomidine continuous infused with 0.2-0.5ug/kg/h

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective laparoscopic major abdominal surgery (laparoscopic pancreaticoduodenectomy, laparoscopic hepatectomy, laparoscopic gastrectomy and laparoscopic enterectomy); 2. Aged 18-65 years; 3. BMI: 18.5-28kg/m^2; 4. The operation time is more than 2 hours; 5. No serious systemic disease; 6. No history of drug allergy.

Exclusion criteria

Exclusion criteria: 1. Patients with distant metastasis and malignant tumors in other organs have received preoperative radiotherapy, chemotherapy or immunotherapy; 2. Patients with autoimmune diseases who have received glucocorticoid or immunosuppressive therapy within 1 year; 3. Severe liver disease, kidney failure or ASA grade IV or above; 4. History of major operation within 1 year; 5. Patients who used opioids before surgery; 6. Pregnant or lactating patients; 7. Long-term use of sedatives, analgesics, chronic alcoholism or drug abuse; 8. Patients with a history of mental illness, language communication disorder, hearing impairment, or inability to understand the test content.

Design outcomes

Primary

MeasureTime frame
Postoperative numeric rating scale pain score;

Secondary

MeasureTime frame
Post-operative quality of recovery scale (PQRS);Postoperative Pittsburgh sleep quality index;Postoperative hospital duration;Complications;Relapse free survival and overall survival;

Countries

China

Contacts

Public ContactZhong Min

Guangdong Provincial Hospital of Chinese Medicine

304637372@qq.com+86 13710011776

Outcome results

None listed

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