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Clinical study of esketamine in postoperative analgesia in HCC patients with TACE

Clinical study of esketamine in postoperative analgesia in HCC patients with TACE

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072923
Enrollment
Unknown
Registered
2023-06-28
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Pain

Interventions

ASI group:PCIA pump: sufentanil 2ug/kg + esketamine 0.5mg/kg
ASII group:PCIA pump: sufentanil 2ug/kg + esketamine 1mg/kg
S group:PCIA pump: sufentanil 3ug/kg

Sponsors

The Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age :30~75 years old; (2)BMI(kg/m2):18~30; (3) American Society of Anesthesiologists (ASA) anesthesia grades:???; (4) Patients diagnosed with hepatocellular carcinoma by abdominal B ultrasound, alpha-fetoprotein examination, liver computed tomography or magnetic resonance imaging; (5) Patients who intend to complete TACE under anesthesia sedation and analgesia; (6) Voluntary participation in the trial; (7) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Preoperative patients with other tumors; (2) Those with uncontrolled hypertension or cardiovascular disease; (3) Fever caused by infection; (4) Mentally ill or uncooperative; (5) Those who are allergic to esketamine; (6) Those who are hearing impaired and unable to cooperate with the completion of the questionnaire; (7) Patients who use painkillers before surgery.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate and severe pain in patients within 72 hours after TACE surgery;

Secondary

MeasureTime frame
VAS scores at the end of surgery, 6h, 24h, 48h, and 72h after surgery;Ramsay sedation scores at the end of surgery, 6h, 24h, 48h, and 72h after surgery;Postoperative recovery quality score (QoR-15) at 24h, 48, and 72h postoperative;Hospital Anxiety and Depression Scale (HADS) scores for 72 hours before and after surgery;

Countries

China

Contacts

Public ContactOu Wei

The Affiliated Hospital of Guizhou Medical University

435719659@qq.com+86 180 9605 7766

Outcome results

None listed

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