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Study on the effect of multimodal general anesthesia based on Butorphanol in laparoscopic gynecological surgery

Anesthesiology

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062343
Enrollment
Unknown
Registered
2022-08-02
Start date
2022-08-05
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Laparoscopic gynecology

Interventions

Butorphanol group:General anesthesia based on butorphanol
The control group:General anesthesia based on fentanyl

Sponsors

The Affiliated Hospital of Medical School of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) 18-65 years old, ASA?-?, BMI<=28kg/m2, scheduled laparoscopic gynecological surgery under general anesthesia, estimated operation time 1-3h; 2) No previous history of abdominal surgery; 3) No history of chronic gastrointestinal diseases.

Exclusion criteria

Exclusion criteria: 1) Use of nsaids within 7 days ; 2) use of opioids within 7 days; 3) pregnancy and lactation; 4) Unable to cooperate; 5) Central nervous system diseases and mental diseases; 6) Operation time >3h; 7) A history of chronic pain; 8) Allergies or contraindications to the drugs used in the study.

Design outcomes

Primary

MeasureTime frame
Postoperative exhaust time;—

Secondary

MeasureTime frame
MAP;HR;VAS;RASS;BIS;Gastrointestinal hormones;—

Countries

China

Contacts

Public ContactZhipeng Xu
xuzhipeng20@163.com+86 18268587893

Outcome results

None listed

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