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A prospective study comparing the onset andanalgesic efficacy of different concentrations levobupivacaine or with dexmedetomidine in young children undergoing caudal blockade

A prospective study comparing the onset andanalgesic efficacy of different concentrations levobupivacaine or with dexmedetomidine in young children undergoing caudal blockade

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002752
Enrollment
Unknown
Registered
2012-11-22
Start date
2012-05-01
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

inguinal hernia andhydrocele in children

Interventions

group L0.25:0.25%levobupivacaine
group L0.20:0.20%levobupivacaine
group LD:0.20%levobupivacaine and 2ug/kg dexmedetomidine

Sponsors

Guangzhou Women andChildrens Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: ASA grade I,II; children aged 1-3 years;children weighing 8-18kg; inguinal hernia andhydrocele in children

Exclusion criteria

Exclusion criteria: children were excluded if they have neurological, neuromuscular, psychiatrics, blood clotting disorders, or a known history of active andsevere renal, hepatic, respiratory of cardiac disease, or a known allergy to local anaesthetics.

Design outcomes

Primary

MeasureTime frame
onset time;postoperative analgesia and the degree of motor block;—

Countries

China

Contacts

Public ContactShe Yingjun
slidekip@163.com+86 13826012672

Outcome results

None listed

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