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the Effect of Dexmedetomidine in Coracoid Approach Brachial Plexus Block

the Effect of Dexmedetomidine in Coracoid Approach Brachial Plexus Block

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02961361
Enrollment
60
Registered
2016-11-11
Start date
2016-11-12
Completion date
2017-05-25
Last updated
2023-02-15

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

Conditions

Injury of Upper Limb

Keywords

dexmedetomidine, coracoid, brachial plexus block

Brief summary

Dexmedetomidine is an α-2 adrenoreceptor agonist and has been extensively used through intravenous infusion,in order to improved the quality of block in regional anesthesia. In this prospective, randomized study, the authors focus on the effect of dexmedetomidine mixed with ropivacaine in coracoid approach brachial plexus block.

Interventions

DRUGropivacaine

40 ml 0.375% ropivacaine was injected after Locating brachial plexus.

DRUGropivacaine mixed with dexmedetomidine

40 ml 0.375% ropivacaine mixed with dexmedetomidine was injected after Locating brachial plexus.

Sponsors

The First Hospital of Qinhuangdao
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. American Society of Anesthesiologists (ASA) physical status I or II; 2. Aged 18-60 years; 3. The elbow, forearm, wrist or hand surgery

Exclusion criteria

1. History of allergy to local anesthetics; 2. Coagulation dysfunction, neuromuscular disease or local infection; 3. The operation time is longer than the local anesthetics effective time.

Design outcomes

Primary

MeasureTime frameDescription
duration timeonce per hour after surgery until 24 hours after surgeryeffective analgesia time

Secondary

MeasureTime frame
onset time5,10,15,20,25,30 min after injection
Visual analogue scale2,6,12,24hour after injection

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026