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Comparative evaluation of butorphanol and dezocine on fentanyl induced cough response during induction of general anesthesia

Comparative evaluation of butorphanol and dezocine on fentanyl induced cough response during induction of general anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023628
Enrollment
Unknown
Registered
2019-06-04
Start date
2019-07-20
Completion date
Unknown
Last updated
2019-06-11

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

Conditions

The fentanyl induced cough response during induction of general anesthesia

Interventions

Group 1:After 3 min of pre-oxygenation, inject intravenously butorphanol 0.03 mg / kg
Group 2:After 3 min of pre-oxygenation, inject intravenously dizocine 0.1 mg / kg
Group 3:After 3 min of pre-oxygenation, inject intravenously Saline 5 ml

Sponsors

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 99 patients underwent gynecologic surgery, aged 18-65 years, with ASA I~II, 18 kg/m2 <BMI <30 kg/m2.

Exclusion criteria

Exclusion criteria: Refusal to participate in this study,undergoing upper respiratory tract infection 2 weeks before surgery, glaucoma, aneurysm, asthma, history of chronic cough, history of smoking, chronic pain and long-term use of analgesics or sedatives, antidepressants, hypertension or long-term use of ace inhibitors.

Design outcomes

Primary

MeasureTime frame
Incidence and severity of the fentanyl induced cough response;

Secondary

MeasureTime frame
Postoperative VAS analgesia score and Ramsay sedation score;Intraoperative hemodynamic parameters;

Countries

China

Contacts

Public ContactHaifa Xia

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

haifaxia@163.com+86 15827639333

Outcome results

None listed

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