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The efficacy of oliceridine combined with remimazolam in percutaneous vertebroplasty for elderly patients with frailty

Efficacy and safety of oliceridine combined with remimazolam in sedation and analgesia during percutaneous vertebroplasty in elderly patients with frailty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124159
Enrollment
Unknown
Registered
2026-05-08
Start date
2026-05-26
Completion date
Unknown
Last updated
2026-05-11

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

Conditions

Thoracolumbar compression fracture

Interventions

Intervention group:oliceridine combined with remimazolam (intervention group): Intravenously inject 1mg of orselenide when turning over
at the beginning of surgery, slowly inject 0.05mg/kg of remazolam intravenously, and then continuously pump 0.1mg/kg/h of remazolam intravenously
Control group:Conventional local anesthesia group (control group): At the same time point, administer an equal dose of placebo (physiological saline) via intravenous injection and pump infusion

Sponsors

Peking University People’s Hospital, Qingdao
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age between 65 and 85 years old, gender not limited; 2. ASA Classification II~III; 3. Body Mass Index (BMI) 18~28 kg/m^2; 4. Frail scale frailty score >= 3 points; 5. Complies with the indications for percutaneous vertebroplasty; 6. Thoracolumbar compression fracture; 7. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Concurrent pulmonary infection; 2. History of allergy to relevant anesthetic drugs; 3. Mental illness or cognitive dysfunction; 4. Hepatic and renal insufficiency; 5. Long-term use of sedative or analgesic drugs.

Design outcomes

Primary

MeasureTime frame
Body movement;

Secondary

MeasureTime frame
Vital signs;Doctor satisfaction;Patient satisfaction;Incidence of intraoperative adverse events ;

Countries

China

Contacts

Public ContactXu Zhang

Peking University People’s Hospital, Qingdao

zx348542767@126.com+86 185 5326 2673

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026