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Side effects of Ed95 butorphanol in gastroenteroscopic anesthesia compared with equivalent sufentanil: a randomized controlled trial

Side effects of Ed95 butorphanol in gastroenteroscopic anesthesia compared with equivalent sufentanil: a randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022780
Enrollment
Unknown
Registered
2019-04-25
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-04-30

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

Conditions

gastroenteroscopic anesthesia

Interventions

Group 1:apply butorphanol for analgesia
Group 2:apply sufentanil for analgesia

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Outpatient of painless gastroenteroscopy; 2. Aged 18 to 65 years; 3. BMI 18.5-30kg/m2; 4. ASA classification from I to III grade; 5. The expecte time of gastroenteroscopy operation is less than 30 minutes.

Exclusion criteria

Exclusion criteria: 1. Exclude heart rate 180mmHg; 2. Exclude acute upper respiratory tract infection; 3. Exclude patients with history of analgesic abuse or analgesic drugs used within half a month. Patients who got thyroid surgery or taking thyroxine drugs were excluded. preoperative weakness, hypokalemia, and myasthenia gravis, relevant drug allergy, gastrointestinal tumors, coagulation abnormalities, hepatic and renal dysfunction, difficult to communicate and cannot cooperate was also excluded.

Design outcomes

Primary

MeasureTime frame
ED95 of butorphanol;the incidence of fatigue;

Secondary

MeasureTime frame
time in postoperative room;dosage of propofol;NRS score;incidence of dizziness;

Countries

China

Contacts

Public ContactXuzhong Xu

The First Affiliated Hospital of Wenzhou Medical University

xuzhong@263.net+86 13706657799

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026