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Application of esmketamine in patient-controlled intravenous analgesia after total hip replacement

Application of esmketamine in patient-controlled intravenous analgesia after total hip replacement

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043649
Enrollment
Unknown
Registered
2021-02-24
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-22

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

Conditions

Total hip replacement

Interventions

control group:Fentanyl intravenous controlled analgesia pump
experimental group :Two dose esketamine intravenous controlled analgesia pumps

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients undergoing unilateral total hip arthroplasty under elective general anesthesia, sex limited, age 18-80 years, ASA class I to III.

Exclusion criteria

Exclusion criteria: Underwent double hip arthroplasty or hip revision; those with severe liver and kidney dysfunction or cardio cerebrovascular disease; those with untreated or inadequately treated hyperthyroidism; those with a previous history of psychiatric disease or unable to cooperate; any known adverse reaction to the drugs used; those on long-term analgesics.

Design outcomes

Primary

MeasureTime frame
Pain score;Use of other analgesic drugs after operation;

Countries

China

Contacts

Public ContactChengxin Lin

The First Affiliated Hospital of Guangxi Medical University

lin.chx@163.com+86 13907865980

Outcome results

None listed

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