Skip to content

Efficacy and safety of Aprepitant and Ondansetron in the prevention of nausea and vomiting after TKA

Efficacy and safety of Aprepitant and Ondansetron in the prevention of nausea and vomiting after TKA

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089511
Enrollment
Unknown
Registered
2024-09-10
Start date
2024-09-30
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Knee osteoarthritis

Interventions

control group:Ondansetron 8mg (4ml: 8mg) was slowly administered intravenously 30 minutes before the end of the procedure (2 minutes).
experimental group:Aprepitant 130mg (18ml:130mg) was slowly administered intravenously 30 minutes before the end of the procedure (2 minutes).

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with severe knee osteoarthritis are eligible for TKA surgery; 2. No cognitive dysfunction or psychiatric history before surgery; 3. Age < 80, no gender limitation; 4. Body weight < 100 kg; 5. ASA score was I-II; 6. Clearly understand and voluntarily participate in the study, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic or intolerant to the experimental drug; 2. Patients with concurrent hepatic and renal insufficiency; 3. Patients with severe intestinal peristalsis; 4. Patients with concurrent arrhythmias, such as atrioventricular block and ventricular arrhythmias 5. Persons with mental disorders;

Design outcomes

Primary

MeasureTime frame
Incidence of PONV at 24h after surgery;

Secondary

MeasureTime frame
The incidence and severity of PONV at 12h, 36h and 48h after operation;VAS score;Time of first postoperative defecation;First time out of bed;Postoperative appetite score;Incidence of treatment-related adverse reactions of grade 1-2 and above;

Countries

China

Contacts

Public ContactFan Lixia

Qilu Hospital of Shandong University

798626623@qq.com+86 185 6008 3758

Outcome results

None listed

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