FindTrial
Sign In

Study on analgesic effect and safety of dexmedetomidine on children after laparoscopic unilateral inguinal ligation

Study on analgesic effect of dexmedetomidine on children after laparoscopic unilateral inguinal ligation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034105
Enrollment
Unknown
Registered
2020-06-24
Start date
2019-03-11
Completion date
Unknown
Last updated
2020-06-29

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

Conditions

Pain after laparoscopic unilateral abdominal ligation of the inguinal canal in children

Interventions

dexmedetomidine group :dexmedetomidine 1.5µg/kg constant speed pump 48 h
dexmedetomidine + sulfentanyl group :dexmedetomidine 1.5µg/kg+ sufentanil 1.5µg/kg constant speed pump 48 h
Sufentanil group :Sufentanil 1.5µg/kg constant speed pump 48 h

Sponsors

Children's Hospital of Baoding City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: 1. Aged 1~3 years 2. Grade of ASA?~ II 3. Undergoing unilateral endocyclic ligation.

Exclusion criteria

Exclusion criteria: 1. Preoperative neurological or cognitive impairment such as epilepsy, depression, dementia, etc. 2. History of psychotropic medication; 3. Abnormal function of heart, liver and kidney; 4. Using vasoactive drugs during the surgery; 5. Allergy to dexmedetomidine or sufentanil; 6. Participate in other drug clinical trials within 3 months.

Design outcomes

Primary

MeasureTime frame
Flacc Pain Score;Sedation score;—

Secondary

MeasureTime frame
vital sign;—

Countries

China

Contacts

Public ContactZhina Liu

Children's Hospital of Baoding

wenwen9604@163.com+86 0312 3377719

Outcome results

None listed

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