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Effects of Intraoperative Continuous Infusion of Low-Dose Dexmedetomidine on Prognosis in Patients Undergoing Elective Neurosurgery: A Single-center, Prospective, Non-Interventional Real-World Study

Effects of Intraoperative Continuous Infusion of Low-Dose Dexmedetomidine on Prognosis in Patients Undergoing Elective Neurosurgery: A Single-center, Prospective, Non-Interventional Real-World Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084903
Enrollment
Unknown
Registered
2024-05-28
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Prognosis for patients undergoing elective surgery in neurosurgery

Interventions

Sponsors

Huzhou Central Hospital, The Affiliated Central Hospital of Huzhou University (The Fifth School of Clinical Medicine of Zhejiang Chinese Medical University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective neurosurgery under general anesthesia; 2. ASA grade I ~ III; 3. Age 18-80 years old, clear mind; 4. Agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who are participating or planning to participate in any interventional clinical trial; 2. Patients with severe hepatic and renal insufficiency; 3. Contraindications to the use of a2-adrenergic agonists; 4. Dexmedetomidine allergy; 5. Severe bradycardia (heart rate <40 beats/min), sick sinus syndrome or second to third degree atrioventricular block; 6. Severe mental illness and communication difficulties; 7. Use amiodarone or dexmedetomidine within 30 days; 8. Ejection fraction < 30% or severe heart failure, myocardial infarction within 7 days.

Design outcomes

Primary

MeasureTime frame
Postoperative recovery time and quality of recovery;

Secondary

MeasureTime frame
The incidence of intraoperative hypotension, the type of vasopressor used and the amount of drugs;Adverse reactions during awakening;The incidence and severity of pain on the day after surgery and within 3-5 consecutive days after surgery, the type and amount of intervention drugs, and the effect after intervention;duration of stay in the postanesthesia care unit;Incidence and severity of delirium on the day after surgery and within 3 to 5 consecutive days after surgery;Recovery on the day after surgery and within 3-5 consecutive days after surgery;Anxiety score on the day after surgery and for 3-5 consecutive days after surgery;Depression score on the postoperative day and for 3-5 consecutive days postoperatively;Sleep quality on the day after surgery and for 3-5 consecutive days after surgery;The incidence, severity and grade of epilepsy, as well as the type and dosage of intervention drugs during postoperative to discharge and within 1 month of postoperative follow-up;

Countries

China

Contacts

Public ContactHe Liu

Huzhou Central Hospital, The Affiliated Central Hospital of Huzhou University (The Fifth School of Clinical Medicine of Zhejiang Chinese Medical University)

lh121061@163.com+86 187 9624 9730

Outcome results

None listed

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