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Effect of esketamine combined with hydromorphone on nausea and vomiting after radical resection of colorectal cancer

Effect of esketamine combined with hydromorphone on nausea and vomiting after radical resection of colorectal cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090806
Enrollment
Unknown
Registered
2024-10-14
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

colorectal cancer

Interventions

control group:Postoperative analgesic intravenous pump: hydromorphone (0.1 mg/kg hydromorphone + 10mg troisetron, diluted to 100 mL with 0.9% normal saline)
intervention group:Intravenous pump for postoperative analgesia: intravenous pump mixed with hydromorphone and esketamine (0.1mg /kg hydromorphone +1mg/kg esketamine + troisetron 10mg, diluted to 100

Sponsors

Peking University Shougang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-75 years old, gender is not limited; (2) Body mass index (BMI) 18-30 kg/m2; (3) American Society of Anesthesiologists (ASA) : Level II-III; (4) Patients who plan to undergo elective laparoscopic radical resection of colorectal cancer under general anesthesia; (5) Receiving patient-controlled intravenous analgesia (PCIA) after surgery; (6) Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Allergy to the drugs used in this study; (2) A history of chronic pain or opioid abuse before surgery; (3) Preoperative history of mental illness or use of antipsychotic drugs; (4) severe heart, brain, liver and kidney diseases (heart failure, myocardial infarction, cerebral infarction, Child-Pugh grade C and renal replacement therapy); (5) untreated or uncontrolled high blood pressure; (6)History of glaucoma, elevated intracranial pressure, hyperthyroidism, or alcoholism.

Design outcomes

Primary

MeasureTime frame
Incidence of PONV within 48 hours after surgery;

Secondary

MeasureTime frame
Postoperative PONV severity score;NRS pain scores at rest and cough within 48 hours after surgery;PACU duration of stay;the satisfaction of patients;Postoperative hospital stay;Number of effective PCIA compressions within 48 hours after surgery;Adverse event within 48 hours after surgery;

Countries

China

Contacts

Public ContactWang Ye

Department of Anesthesiology, Peking University Shougang Hospital

minami01@163.com+86 138 1038 6807

Outcome results

None listed

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