Skip to content

Effect of intraoperative esketamine infusion on early recovery quality and emotional state of patients undergoing percutaneous nephrolithotomy

Effect of intraoperative esketamine infusion on early recovery quality and emotional state of patients undergoing percutaneous nephrolithotomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097821
Enrollment
Unknown
Registered
2025-02-26
Start date
2024-08-26
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Urinary calculus

Interventions

Esketamine group:Intravenous injection 0.25mg/Kg esketamine
Normal saline group:Use the same dose of saline

Sponsors

The Second Affiliated Hospital of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I - II 2. Age 18-80 years old 3. Patients undergoing percutaneous nephrolithotomy at selected time 4. BMI 18-30;

Exclusion criteria

Exclusion criteria: 1.Patients with surgical contraindications, such as coagulation dysfunction, infectious diseases, immune diseases, etc. 2.Patients with severe malignant tumors or cardiovascular and cerebrovascular diseases; 3.Hypertension is poorly controlled 4.Patients with mental or nervous system diseases; Pregnant or lactating women or subjects (including men) who plan to have a baby within 6 months; 5.Allergic to narcotic drugs; 6.Unwilling to participate in the experiment, clinical data lost;

Design outcomes

Primary

MeasureTime frame
Postoperative Recovery Scale -40 score;Self-rating anxiety scale;Self-rating depression Scale;

Secondary

MeasureTime frame
Mean arterial pressure, MAP;Operation time;Respiratory recovery time (from withdrawal of anesthesia to recovery of spontaneous respiration);VAS pain score ;Postoperative adverse reactions (including nausea and vomiting, dreaminess, nightmares, dizziness and headache);Age;Extubation time (from withdrawal of anesthesia Time to extubation);Sex;ASA rating;BMI;Propofol dosage;Remifentanil dosage;Vasoactive drug use;Remedy the analgesic condition during PACU;

Countries

China

Contacts

Public ContactZhang Yongfa

The Second Affiliated Hospital of Shantou University Medical College,Department of Anesthesiology

259395234@qq.com+86 137 5045 3746

Outcome results

None listed

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