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Observation of the efficacy and safety of ? receptor analgesic drug nalbuphine in patients with multiple injuries: a clinical single-center prospective randomized controlled trial

Observation of the efficacy and safety of ? receptor analgesic drug nalbuphine in patients with multiple injuries: a clinical single-center prospective randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046500
Enrollment
Unknown
Registered
2021-05-17
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

Multiple injuries

Interventions

Group TI:I.V. Nalbuphine Hydrochloride 100ug/kg/h
Group T2:I.V. Remifentanil Hydrochloride 0.5ug/kg/h
Group T3:I.V. Nalbuphine Hydrochloride 100ug/kg/h+Remifentanil Hydrochloride 0.5ug/kg/h

Sponsors

The Third Affiliated Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Clinical diagnosis of multiple injuries, two doctors who have been engaged in emergency and severe illness for more than 2 years jointly evaluate patients who need continuous analgesia, and the continuous analgesia time is >= 48h; 2. Aged 18-65 years old; 3. Survival time > 2 weeks.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to opioids; 2. Patients with bradycardia (heart rate <= 50 beats /min), ? degree ATrioventricular block, systolic blood pressure <90 mmHg; 3. Pregnant or lactating women; 4. Patients with a history of mental illness; 5. Patients with severe liver and kidney insufficiency, severe brain stem failure, and severe cardiopulmonary dysfunction; 6. Endocrine disorders, acute and chronic neuromuscular diseases, and diseases of the blood system; 7. Patients with malignant tumor and pain, history of long-term analgesic use, history of chronic pain; 8. Patients considered unsuitable for clinical trials by the investigator.

Design outcomes

Primary

MeasureTime frame
The amount of morphine required to maintain the ideal analgesic effect (COPT 0-1 points) for each group of patients;

Secondary

MeasureTime frame
Duration of mechanical ventilation;Duration of ICU stay;Duration of hospital;Inflammatory mediator level;

Countries

China

Contacts

Public ContactGu Zhengtao

The Third Affiliated Hospital of Southern Medical University

648817770@qq.com+86 13631419057

Outcome results

None listed

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