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Clinical study on perioperative analgesia of butorphanol in patients with ovarian cancer

Clinical study on perioperative analgesia of butorphanol in patients with ovarian cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069879
Enrollment
Unknown
Registered
2023-03-28
Start date
2023-04-25
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

ovarian cancer

Interventions

Group 1:Sufentanil 0.04 µg·kg-1·h-1
Group 2:Butorphanol 3.0ug·kg-1·h-1
Group 3:Butorphanol 3.5ug·kg-1·h-1
Group 4:Butorphanol 4.0ug·kg-1·h-1

Sponsors

The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA level I - III; 2. Patient compliance is good; 3. Ovarian cancer confirmed by postoperative pathologic diagnosis and receive cytoreductive surgery; 4. No history of related drug allergies; 5. FIGO classification I-III; 6. Age 18-65 years old.

Exclusion criteria

Exclusion criteria: 1. Patients with multiple chronic diseases who cannot tolerate surgical anesthesia; 2. Severe heart, lung, and kidney dysfunction; 3. Coagulation dysfunction; 4. Individuals with drug allergies and contraindications; 5. Patients with severe sequelae of neurological disorders; 6. Patients with advanced malignant tumors; 7. Previous or recent history of taking opioid drugs; 8. Recent new infections or immune system diseases; 9. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale/Score,;

Secondary

MeasureTime frame
Adverse reactions;Rescue analgesia;CD4+ T lymphocyte;CD8+ lymphocyte;CA-125;HE4;Inflammatory factor;

Countries

China

Contacts

Public ContactWei Zhang

The First Affiliated Hospital of University of Science and Technology of China (Anhui Provincial Hospital)

zw97079@163.com+86 138 5604 2616

Outcome results

None listed

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