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Application of oliceridine to inhibit sufentanil-induced cough response

Application of oliceridine to inhibit sufentanil-induced cough response

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095936
Enrollment
Unknown
Registered
2025-01-15
Start date
2025-01-31
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Sufentanil-induced cough

Interventions

Experimental group:1.5 mg of oliceridine is diluted to 5 ml intravenously for 1 min before induction
Control group:Normal saline 5ml slow intravenous injection

Sponsors

The Second People's Hospital of Hefei
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) ASA anesthesia classification I.~II.; (2) The patient was 18 years old<= age <= 65 years old, BMI: 18-25kg/m²; (3) Patients undergoing elective general anesthesia surgery (4) The patients voluntarily participated in this study and had signed the informed consent form before surgery.

Exclusion criteria

Exclusion criteria: (1) Patients who are allergic to oliceridine and other anesthetic drugs; (2) History of severe postoperative nausea and vomiting; (3) Patients with impaired language, intelligence, comprehension and inability to communicate normally; (4) Patients with a history of neuropsychiatric disorders, drug dependence, and alcoholism; (5) Patients with severe cardiovascular and cerebrovascular diseases or preoperative dysfunction of major organs; (6) The patient's electrocardiogram is abnormal, such as QT interval prolongation >450ms.

Design outcomes

Primary

MeasureTime frame
Choking score;

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;Pulse oximetry;

Countries

China

Contacts

Public ContactQuanmin Chen

The Second People's Hospital of Hefei

3261582395@qq.com+86 182 9762 1390

Outcome results

None listed

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