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95% effective dosage of infusion esketamine in ureteral stent removal

95% effective dosage of infusion esketamine in ureteral stent removal

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062077
Enrollment
Unknown
Registered
2022-07-21
Start date
2022-07-23
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

ureteral stent removal

Interventions

Sponsors

The Second Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The inclusion criteria were Society of Anesthesiologists (ASA) physical status I-III patients, the gender not limited,aged between 18-65 years who were scheduled for elective ureteral stent removal in the Second Affiliated Hospital of Chongqing Medical University.

Exclusion criteria

Exclusion criteria: The exclusion criteria included a significant renal or hepatic dysfunction, a known neuromuscular disease, habitual sedative or analgesic use,allergy to any study medications, chronic hypertension without regular treatment, hypoproteinemia and devoid of postoperative telephone access.

Design outcomes

Primary

MeasureTime frame
a valid inhibition of body movement.;

Secondary

MeasureTime frame
heart rate,blood pressure,SPO2;Aldrete score;

Countries

China

Contacts

Public ContactShu Shiyu

The Second Affiliated Hospital of Chongqing Medical University

514712760@qq.com+86 18917785284

Outcome results

None listed

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