FindTrial
Sign In

Intraoperative dexmedetomidine infusion improved emergence agitation and quality of recovery in adults after lung surgery:a retrospective cohort study

Intraoperative dexmedetomidine infusion improved emergence agitation and quality of recovery in adults after lung surgery:a retrospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RRC-17013603
Enrollment
Unknown
Registered
2017-11-29
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

medicine effect

Interventions

1:Dexmedetomidine
2:nondexmedetomidine

Sponsors

the First Affiliated Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Adults (=18 years); lung surgery under general anaesthesia; elective surgery

Exclusion criteria

Exclusion criteria: requiring reoperation due to serious postoperative complications; directly admitted to ICU after surgery; patients with incomplete information, influencing the identification of efficacy and safty

Design outcomes

Primary

MeasureTime frame
Emergence agitation;—

Secondary

MeasureTime frame
Postoperative pain score;Shivering;—

Countries

China

Contacts

Public ContactKang Xianhui

the First Affiliated Hospital, College of Medicine, Zhejiang University

kxhui66@126.com+86 13738135290

Outcome results

None listed

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