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Comparison of intranasal and intravenous dexmedetomidine for prevention of post spinal shivering in patients undergoing lower limb orthopedic surgery

Comparison of intranasal and intravenous dexmedetomidine for prevention of post spinal shivering in patients undergoing lower limb orthopedic surgery - dexmedetomidine and shivering

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042760
Enrollment
120
Registered
2020-12-28
Start date
2020-12-28
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients undergoing elective lower limb orthopedic surgeries under subarachnoid blockade were recruited into the study.

Interventions

In group C, normal saline was administered intranasally 40 min before spinal anesthesia and intravenously 30 min following nasal medication, respectively. In group V, normal saline was administered in

Sponsors

Department of Anaesthesiology, People's Hospital of Chongqing Banan District
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adult patients (ASA grades I to II) scheduled for elective lower limb orthopedic surgery under subarachnoid blockade were included in this study.

Exclusion criteria

Exclusion criteria: 1, obese; 2, taking vasoactive or antidepressant drugs, receiving intraoperative blood or blood products transfusion; 3, with cardiac disease (heart blocks, bradyarrhythmias, and left ventricular failure), renal disease, hepatic disease, psychiatric disorder, neuropathies or severe diabetic autonomic neuropathy; 4, known history of substance or alcohol abus; 5, with a contraindication to regional anesthesia; 6, known allergy or hypersensitivity to dexmedetomidine and local anaesthetics; 7, history of nasal operation and nasal diseases, including rhinitis, nasal polyp, and nasosinusitis; 8, cardiovascular comorbidity, including bradycardia and atrioventricular block;

Design outcomes

Primary

MeasureTime frame
The primary outcomes were the incidence and intensity of shivering.

Countries

Asia(except Japan)

Contacts

Public Contactjie Chen

People's Hospital of Chongqing Banan District Department of Anaesthesiology

cjandsh@tmmu.edu.cn+81-086-23-66234145

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026