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Evaluation of multimodal analgesia of nalbuphine combined with flurbiprofen axate after laparoscopic hepatectomy: a multicenter, prospective trial

Evaluation of multimodal analgesia of nalbuphine combined with flurbiprofen axate after laparoscopic hepatectomy: a multicenter, prospective trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044538
Enrollment
Unknown
Registered
2021-03-23
Start date
2021-04-20
Completion date
Unknown
Last updated
2021-09-20

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

Conditions

Primary liver cancer

Interventions

Nalbuphine group:4h after surgery, nalbuphine 0.2mg/Kg was mixed with 100ml normal saline, 40-50 drops/min, TID (8h/ time), for 72h.
Pentazocine group:4h after the operation, the patient was given 30mg pentazocin mixed with 100ml normal saline, 40-50 drops/min, Bid, for 72h.
flurbiprofen axetil group:Flurbiprofen ester (100mg for analgesia) was given 4h after surgery and mixed with 100ml normal saline, 40-50 drops/min, Bid, for 72h.
Nalbuphine and flurbiprofen axetil group:4h after surgery, flurbiprofen ester was given 50mg for analgesia, supplemented with 100ml normal saline, 40-50 drops/min, Bid, and nalbuphine 0.1mg/Kg, supple
pentazocine and flurbiprofen axetil group:4h after surgery, flurbiprofen ester was given 50mg for analgesia mixed with 100ml normal saline intravenous drip, 40-50 drops/min, Bid, and tetazocine 15mg m

Sponsors

Tongji Hospital,Tongji Medical College of Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are planning to undergo laparoscopic liver resection; 2. ASA I-III ; 3. Aged = 18 years, voluntarily sign an informed consent form; 4. Body weight 40-90 kg.

Exclusion criteria

Exclusion criteria: 1. People who are allergic to nalbuphine hydrochloride or its components, patients with a history of opioid allergy; 2. History of neurological diseases; 3. History of chronic pain; 4. Drug addiction and alcoholism; 5. History of long-term use of opioids; 6. Patients with coronary heart disease, bronchial asthma, severe hypertension, severe blood system dysfunction, liver and kidney function, and electrolyte abnormalities; 7. Those who have poor compliance and cannot cooperate with surgery; 8. Those who have participated in clinical trials of other drugs in the past 4 weeks; 9. Accompanied by other conditions, the investigator believes that it is not suitable for selected patients.

Design outcomes

Primary

MeasureTime frame
VAS pain score;Postoperative adverse reactions (PONV);

Secondary

MeasureTime frame
Inflammatory factors;

Countries

China

Contacts

Public ContactZhang Lei
zhangl7803@126.com+86 13886171160

Outcome results

None listed

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