Skip to content

Comparison of the analgesic effects of dexmedetomidine combined with different opioids for single-vertebra percutaneous vertebroplasty in elderly patients

Comparison of the analgesic effects of dexmedetomidine combined with different opioids for single-vertebra percutaneous vertebroplasty in elderly patientsComparison of the analgesic effects of dexmedetomidine combined with different opioids for single-vertebra percutaneous vertebroplasty in elderly patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112302
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Intraoperative Pain Management for Osteoporotic Spinal Compression Fractures in the Elderly

Interventions

Dexmedetomidine group (Group D):Inject 5ml of saline intravenously 5 minutes before the surgery.
Dexmedetomidine and Sufentanil Group (DS Group):Administer 5ml of sufentanil containing 0.1 µg/kg intravenously 5 minutes before surgery.
Dexmedetomidine-Nalbuphine Group (DN Group):Administer 5ml of intravenous nalbuphine at 0.1mg/kg 5 minutes before the surgery.

Sponsors

Central Hospital of Dalian University of Technology (Dalian Municipal Central Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients undergoing single vertebroplasty; 2. Age >65 years; 3. ASA class I-III; 4. BMI 18-28 kg/m^2; 5. Signed informed consent

Exclusion criteria

Exclusion criteria: 1. Patients unable to complete the scale assessment; 2. History of psychiatric disorders, chronic pain, or alcohol or drug abuse; 3. Severe dysfunction of the heart, lungs, liver, or kidneys (transaminase levels increased by 2 times or more); 4. Allergic to the study drug; 5. Preoperative PaO2 < 60 mmHg or SpO2 < 92%; 6. Participation in another drug clinical trial within the past 30 days.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Systolic Blood Pressure;Diastolic Blood Pressure;Mean arterial pressure;Heart rate;Pulse oxygen saturation;Ramsay Sedation Scale;Dosage of vasoactive drugs;Number of times vasoactive drugs are used;3D-CAM Scale;Qor-15;Patient pain satisfaction;Postoperative Pain Satisfaction;Incidence of moderate to severe pain;Adverse reaction;

Countries

China

Contacts

Public ContactCongjie Bi;Naying Su

Central Hospital of Dalian University of Technology (Dalian Municipal Central Hospital)

congjie.bi@outlook.com+86 135 0425 1513

Outcome results

None listed

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