Skip to content

Effects of dexmedetomidine combined with ropivacaine for ultrasound-guided brachial plexus nerve block in children

Effects of dexmedetomidine combined with ropivacaine for ultrasound-guided brachial plexus nerve block in children

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045358
Enrollment
Unknown
Registered
2021-04-13
Start date
2021-04-20
Completion date
Unknown
Last updated
2021-11-22

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

Conditions

Pediatric patients

Interventions

C group:0.3% ropivacaine was used for brachial plexus block
DL1 group:Dexmedetomidine 0.75 µg/kg+0.3% ropivacaine was used for brachial plexus block
DL2 group:Dexmedetomidine 1 µg/kg+0.3% ropivacaine was used for brachial plexus block
DL3 group :Dexmedetomidine 1.25 µg/kg+0.3% ropivacaine was used for brachial plexus block

Sponsors

Jiangsu Province Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 1-3 years, weighing 6.1-18 kg; 2. ASA grade I-II; 3. Children who intend to block the upper limbs under general anesthesia + unilateral intermuscular brachial plexus block.

Exclusion criteria

Exclusion criteria: 1. Have a history of surgery in the area innervated by the ipsilateral brachial plexus or have received block anesthesia for the ipsilateral brachial plexus; 2. Neuromuscular dysfunction; 3. Have a diagnosed mental illness or suffer from epilepsy; 4. Possess coagulation dysfunction; 5. The legal guardian of the child refused to participate in the study.

Design outcomes

Primary

MeasureTime frame
Duration of sensory block;

Secondary

MeasureTime frame
Duration of motion block;Operation time;recovery time;effect of nerve block;Additional vasoactive drug doses;Additional dose of analgesic medication;

Countries

China

Contacts

Public ContactHe Mingfeng

Jiangsu Province Hospital

18551682286@126.com+86 18551682286

Outcome results

None listed

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