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The effect of preoperative application of dexmedetomidine on intraoperative awakening quality in children undergoing strabismus correction

The effect of preoperative application of dexmedetomidine on intraoperative awakening quality in children undergoing strabismus correction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107233
Enrollment
Unknown
Registered
2025-08-06
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Pediatric strabismus

Interventions

Experimental group:Dosage: 30 mim administration before surgery 10.7kg<=body weight< 19.4kg Use 1ml: 300µg specification (15µg per spray), sprayed through the nasal cavity, 1 spray on each side of the
Control group:Usage and dosage: Nasal drip 30 minutes before surgery Equal dose of physiological saline solution

Sponsors

Kaifeng Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1. Age 2-14 years old, gender is not limited; 2. American Anesthesiologist Classification (ASA) I-II; 3. Children who need general anesthesia for elective surgery; 4. BMI 18~25 kg /m^2, good growth and development.

Exclusion criteria

Exclusion criteria: 1. Children who are allergic to the anesthetic used for this operation; 2. Children with respiratory tract infection, central nervous system, heart, lung, and brain diseases; 3. Children with incomplete information or difficulty in cooperating with examination and surgery; 4. Preoperative consciousness disorders, cognitive disorders, and communication disorders.

Design outcomes

Primary

MeasureTime frame
Wake-up time;Wake-up time;

Countries

China

Contacts

Public ContactWeizhong He

Kaifeng Central Hospital

xin20200202@126.com+86 371 2567 2543

Outcome results

None listed

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