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Effect of esketamine on hip replacement patients on postoperative pain, depression and recovery

Effect of esketamine on hip replacement patients on postoperative pain, depression and recovery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031960
Enrollment
Unknown
Registered
2020-04-16
Start date
2020-05-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Total hip arthroplasty

Interventions

Group K1:Perioperative use of esketamine
Group K2:Perioperative and postoperative analgesia pumps use of esketamine

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients to be treated with hip replacement; 2. Patients with ASA grade I-III; 3. Patients aged 45-75 years; 4. Patients with body mass index (BMI) < 30; 5. Patients willing to sign informed consent of anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with bone tumor; 2. Patients who are allergic to the study drug; 3. Patients with severe hypertension and liver and kidney dysfunction; 4. Patients with long-term opioid use, alcohol or drug abuse; 5. Patients with consciousness disorder or severe mental and nervous system diseases.

Design outcomes

Primary

MeasureTime frame
VAS score;Postoperative analgesic pump dosage;Patien Health Questionnare;Generalized Anxiety Disorder, GAD-7;Postoperative recovery;

Secondary

MeasureTime frame
Plasma inflammatory factor levels;Nausea, headache, dizziness, blurred vision, hallucinations, nightmares;

Countries

China

Contacts

Public ContactAi Yan-qiu

The First Affiliated Hospital of Zhengzhou University

aiyanqiu@163.com+86 13607690334

Outcome results

None listed

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