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Impact of Nalbuphine on Postoperative Analgesia in Elderly Patients Undergoing Total Hip Arthroplasty under the ERAS Concept

Impact of Nalbuphine on Postoperative Analgesia in Elderly Patients Undergoing Total Hip Arthroplasty under the ERAS Concept

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121773
Enrollment
Unknown
Registered
2026-04-02
Start date
2026-04-02
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Postoperative pain

Interventions

Nalbuphine Group:Nalbuphine postoperative analgesia

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 65 - 85 years old; 2. Total hip replacement surgery under elective general anesthesia; 3. ASA classification: II - III; 4. No communication disorder, clear consciousness; 5. BMI: 18.5 - 28 kg/m^2; 6. Voluntary use of postoperative intravenous analgesia device; 7. Compliant with ethics, the patient voluntarily participates and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to opioids or study drugs. 2. Those with severe liver or kidney dysfunction, history of asthma or chronic obstructive pulmonary disease. 3. Those who have been taking opioids for a long time or have a history of drug abuse. 4. Those with severe gastric ulcers, coagulation dysfunction or surgical site infections. 5. Those with language disorders or mental illnesses who are unable to communicate. 6. Those who refuse to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
NRS score at 24 hours after surgery;

Secondary

MeasureTime frame
Adverse event;The incidence of postoperative nausea and vomiting within three days after the operation;The incidence rate of postoperative delirium (POD) within three days after surgery;The NRS scores at 48 hours and 72 hours after the operation;

Countries

China

Contacts

Public ContactYu Qi

Xuzhou Central Hospital

597562326@qq.com+86 516 8395 6183

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026