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Effects of Esketamine Combined with Butorphanol Tartrate for Postoperative Analgesia on Postoperative Nausea and Vomiting in Female Patients After Thoracic Surgery.

Effects of Esketamine Combined with Butorphanol Tartrate for Postoperative Analgesia on Postoperative Nausea and Vomiting in Female Patients After Thoracic Surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114533
Enrollment
Unknown
Registered
2025-12-15
Start date
2025-12-20
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Pulmonary nodule,Lung cancer,Mediastinal mass

Interventions

B Group(Esketamine combined with Butorphanol tartrate PCA group):The solution for Group B contained esketamine 1.0mg/kg and butorphanol tartrate 8-12mg. For both groups, ramosetron 0.9mg was added, an
S Group (Esketamine Combined with Sufentanil PCA group)):In the esketamine (1.0 mg/kg) and sufentanil (1.5 µg/kg) groups, ramosetron 0.9 mg was added to each patient-controlled analgesia (PCA) pump an

Sponsors

The Second Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients undergoing thoracic surgery under general anesthesia with postoperative PCA; 2.Female patients aged 18–80 years; 3.ASA physical status classification I–III; 4. BMI 18–28 kg/m^2; 5. No severe cardiovascular disease, hepatic or renal dysfunction, or impaired consciousness before surgery; 6.Fully awake with restored orientation, cooperative with physical examination, and able to communicate normally at 6 hours postoperatively; 7. Patients who provided informed consent for this study.

Exclusion criteria

Exclusion criteria: 1. Severe hepatic or renal dysfunction, or severe cardiovascular and cerebrovascular diseases; 2. Postoperative admission to the ICU; 3. History of psychiatric disorders or preoperative cognitive impairment; 4.Postoperative agitation, impaired consciousness, or inability to cooperate; 5.Long-term use of opioid analgesics or other pain-relief medications; 6.Incomplete or missing postoperative follow-up records; 7.Unwillingness to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Nausea and Vomiting Scale;Incidence of nausea and vomiting;

Secondary

MeasureTime frame
Pain score;Sedation Score;Adverse Event;Time to First Flatus;The first time you walk after surgery;48-hour analgesic pump effective presses;Number of rescue analgesic dose;48-hour analgesic pump effective presses;Incidence of postoperative complications;

Countries

China

Contacts

Public ContactZhou Feng

The Second Hospital of Dalian Medical University

zhou6dl@163.com+86 177 0987 1766

Outcome results

None listed

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