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Intraoperative dexmedetomidine for sedation and postoperative pain management in patients undergoing lumbar discectomy

Intraoperative dexmedetomidine for sedation and postoperative pain management in patients undergoing lumbar discectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003645
Enrollment
Unknown
Registered
2013-09-28
Start date
2013-09-29
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Anesthesia of orthopedics

Interventions

dexmedetomidine group:dexmedetomidine
control group:midazolam

Sponsors

Department of Anesthesiology, First Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients between the ages of 18 and 65 years with ASA classification17 of I or II undergoing lumbar discectomy with epidural anesthesia were eligible for inclusion in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria were known allergy to a-2 agonists, ASA classification III or more, respiratory problems (pneumonia, asthma, bronchitis and severe obstructive sleep apnea), sinus bradycardia(<50bpm), severe arrhythmia.

Design outcomes

Primary

MeasureTime frame
hemodynamic changes;sedation scores;pain scores;PONV scores;satisfaction score;—

Countries

China

Contacts

Public ContactKe Peng

First Hospital of Soochow University

pengke0422@163.com+86 15962155989

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026