Study on the effect of multimodal general anesthesia based on Butorphanol in intestinal paralysis after gastrointestinal surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200064555

Enrollment

Unknown

Registered

2022-10-11

Start date

2022-10-10

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

laparoscopic gastrointestinal surgery

Interventions

Group 1 :General anesthesia based on butorphanol

Group 2:General anesthesia based on fentanyl

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years old, ASA I-III, BMI <= 28 kg/m2, planning to undergo elective laparoscopic gastrointestinal surgery under general anesthesia, and the estimated operation time is < 4 hours; 2. No history of abdominal surgery; 3. No history of chronic gastrointestinal diseases in the past.

Exclusion criteria

Exclusion criteria: 1. Apply non-steroidal anti-inflammatory drugs within 7 days; 2. Use opioids within 7 days; 3. Pregnancy and lactation; 4. Unable to cooperate; 5. Central nervous system diseases and mental diseases; 6. Operation time > 3 hours; 7. Have a history of chronic pain; 8. Allergic to the drugs used in the test or have contraindications.

Design outcomes

Primary

Measure	Time frame
Postoperative exhaust time;Delayed anal exhaust;	—

Secondary

Measure	Time frame
Anal defecation;Bowel sounds;	—

Countries

China

Contacts

Public ContactZhipeng Xu

The Affiliated Hospital of Medical School of Ningbo University

xuzhipeng20@163.com+86 18268587893

Outcome results

None listed

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