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The Impact of Neoadjuvant Therapy on the Intraoperative Remifentanil Dosage in Esophageal Cancer Patients: A Prospective Observational Study Based on the IoC

The Impact of Neoadjuvant Therapy on the Intraoperative Remifentanil Dosage in Esophageal Cancer Patients: A Prospective Observational Study Based on the IoC

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500105958
Enrollment
Unknown
Registered
2025-07-15
Start date
2025-07-15
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Esophageal Cancer

Interventions

Sponsors

Department of Anesthesiology, Affiliated Cancer Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing radical resection of esophageal cancer under cervical and abdominal thoracoscopy under intravenous anesthesia at the elective stage 2. Age>=65 years 3.BMI18.5~28kg/m^2 4. ASAII.~III

Exclusion criteria

Exclusion criteria: 1. Long-term use of psychotropic drugs or sedative analgesics before surgery. 2. History of allergy to any of the drugs used in this study. 3. Cognitive dysfunction before surgery (positive score on the preoperative 3D-CAM assessment). 4. History of brain diseases or head trauma. 5. Severe preoperative liver or kidney dysfunction or severe cardiac insufficiency (NYHA Class IV). 6. History of other cancer treatments. 7. Participation in other studies within the past three months.

Design outcomes

Primary

MeasureTime frame
The average intraoperative dose of remifentanil;

Secondary

MeasureTime frame
Postoperative delirium;Intraoperative opioid dosage (converted to morphine equivalent);Total postoperative opioid consumption (converted to morphine equivalents);Visual analogue scale (VAS) pain scores at rest and during activity on postoperative days 1, 2, and 3.;Use of rescue analgesics and pain medications by patients on postoperative days 1, 2, and 3.;Postoperative hospital stay duration;The number of effective presses and the total number of presses on the patient-controlled intravenous analgesia (PCIA) pump postoperatively.;

Countries

China

Contacts

Public ContactZhang Minhao

Department of Anesthesiology, Affiliated Cancer Hospital of Nanjing Medical University

zhangminhao@njmu.edu.cn+86 153 3515 8002

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 31, 2026