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The comperative effects of dexmedetomidine and magnesium sulfate as adjuvant of local anesthetics for ultra-sound guided axiliary brachial plexus block

The comperative effects of dexmedetomidine and magnesium sulfate as adjuvant of local anesthetics for ultra-sound guided axillary brachial plexus block

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16007742
Enrollment
Unknown
Registered
2016-01-12
Start date
2016-01-01
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

surgeries of hand and forearm

Interventions

Group D:Solutions for brachial plexus block:(0.25% ropivacain+1% lidocaine) 30ml+ 0.75µg/kgdexmedetomidine 3ml
Group M:Solutions for brachial plexus block:(0.25% ropivacain+1% lidocaine) 30ml+150mg magnesium sulfate 3ml
Group C:(0.25% ropivacaine+1%lidocaine) 30ml+NS 3ml

Sponsors

the Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: patients scheduled for forearm or hand surgery undergoing the ultra-sound guided axillary brachial plexus block and ASA status I-II.

Exclusion criteria

Exclusion criteria: patients with a history of allergy to the study medication, peripheral neuropathy, central nervous system disease, puncture site infection, a history of severe heptic, renal, cardiac or pulmonary disease, coagulation disorder, alcohol or opioid abuse, chronic pain, severe morbid obesity, pregnancy or lactating women

Design outcomes

Primary

MeasureTime frame
the onset time of sensory block;the onset time of motor block;the duration of sensory block;the duration of motor block;the duration of motor block;the analgesic time;the analgesics assumption 24h after surgery;

Secondary

MeasureTime frame
BIS values;

Countries

China

Contacts

Public ContactWenzhi Li
wenzhili9@126.com+86 18045159998

Outcome results

None listed

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