Skip to content

Randomized controlled clinical study of hydromorphone combined with nalbuphine for intravenous controlled analgesia in patients after partial hepatectomy

Randomized controlled clinical study of hydromorphone combined with nalbuphine for intravenous controlled analgesia in patients after partial hepatectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092078
Enrollment
Unknown
Registered
2024-11-08
Start date
2024-11-20
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Partial hepatectomy

Interventions

H Group: H: hydromorphone 10mg
HN Group:HN: hydromorphone 10mg+ Nalbuphine 50mg

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Patients who are expected to treated with controlled intravenous analgesia after elective laparoscopic partial hepatectomy; 2) ASAI-III level; 3) Age 18 or older, regardless of gender. 4) No communication barriers, able to understand the study process and the use of pain scales, and able to operate self-controlled analgesia equipment; 5) Voluntarily participated and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) Participants who have participated in other drug clinical trials within the last 3 months; 2) Those who have taken monoamine oxidase inhibitors or antidepressants within 15 days; Psychiatric disorders (schizophrenia, mania, bipolar disorder, psychosis, etc.), and a history of long-term use of psychotropic drugs 3) Patients with chronic pain who have research related drug allergies, long-term use of opioids, or drug addiction; 4) Patients with a history of severe digestive disorders (known or suspected gastrointestinal obstruction, including paralytic ileus), severe respiratory depression, and asthma 5) Patients who cannot express their wishes correctly; Poor compliance, unable to complete the experiment according to the study protocol; 6) Patients transferred to ICU after surgery; 7) Pregnant or lactating women; 8) Researchers consider it inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
Nausea and vomiting;

Secondary

MeasureTime frame
NRS pain score;

Countries

China

Contacts

Public ContactLIUFEI

West China Hospital of Sichuan University

30333870@qq.com+86 189 8060 5856

Outcome results

None listed

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