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Effects of single-dose dexmedetomidine on emergence agitation from sevoflurane anaesthesia in patients undergoing gynecological laparoscopic surgery

Effects of single-dose dexmedetomidine on emergence agitation from sevoflurane anaesthesia in patients undergoing gynecological laparoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021004
Enrollment
Unknown
Registered
2019-01-24
Start date
2019-01-28
Completion date
Unknown
Last updated
2019-01-28

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

Conditions

Emergence Agitation

Interventions

Group 1:dexmedetomidine administered IV over 15 minutes after induction
Group 2:NS administered IV over 15 minutes after induction

Sponsors

West China Second Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. aged 18-40 years; 2. ASA physical status I and II; 3. scheduled for elective gynecological laparoscopic surgery; 4. with no contraindication to dexmedetomidine; 5. voluntary to participate in the clinical study.

Exclusion criteria

Exclusion criteria: 1. patients with pulmonary, cardiac, renal, hepatic, cerebrovascular, or psychiatric diseases; 2. refused to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Emergence Agitation Score;—

Secondary

MeasureTime frame
VAS Score;—

Countries

China

Contacts

Public ContactMin Diao

West China Second Hospital, Sichuan University

1988228cd@163.com+86 15982112792

Outcome results

None listed

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