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Prospective Clinical Trial Comparing Infraclavicular Versus Axillary Approach to Brachial Plexus Block

Prospective Randomized Clinical Trial Comparing Infraclavicular Versus Axillary Approach to Brachial Plexus Block.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02208245
Enrollment
46
Registered
2014-08-05
Start date
2014-02-28
Completion date
2015-03-31
Last updated
2014-08-05

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

Conditions

Distal Radius Fractures, Scaphoid Fractures, Wrist Injury Arthrodesis

Brief summary

The brachial plexus block is an anesthetic technique often used for surgical procedures of the upper limb. To get the brachial plexus block, several routes can be used, including the axillary and infraclavicular approach. Few studies have compared these techniques, considering the time to perform the block, the onset time and success rate, with conflicting results. Furthermore, there is little information in the literature comparing the length of postoperative analgesia provided by these techniques. Therefore, the investigators designed this study in order to elucidate the differences between these two techniques to assist the anesthesiologist to choose the best of them in clinical practice.

Interventions

DEVICEUltrasound: Infraclavicular block

Ultrasound guided infraclvicular block

DRUGRopivacaine

20 ml of ropivacaine 0,5% in both groups ( axillary block and infraclavicular block)

DEVICEUltrasound: Axillary block

Ultrasound guided axillary block

Sponsors

Federal University of São Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* age older than 18 years and less than 70 years * consent informed signed by the patient * candidates for surgical intervention of scaphoid fractures, distal radius fractures and wrist arthrodesis * American Society of Anesthesiology physical status I, II and III * body mass index (BMI) \<35 kg / m².

Exclusion criteria

* cognitive impairment or active psychiatric condition * infection at the puncture site * bleeding disorders * history of allergy to ropivacaine

Design outcomes

Primary

MeasureTime frameDescription
postoperative analgesiafirst postoperative dayAll patients will be contacted on the first postoperative day to tell the time of onset of pain postoperatively. The duration of postoperative analgesia is defined as the interval between the end of local anesthetic injection and the onset of postoperative pain reported by the patient.

Secondary

MeasureTime frameDescription
local anesthetic pharmacokineticsDuring the procedureVenous blood samples will be taken from some patients through a cannula. The samples will be used for the determination of serum levels achieved after ropivacaine blockade. Samples will be taken every 15 minutes during the first hour, every 30 minutes during the second hour and 4 hours after the blockade. These samples will be analyzed using the technique of high performance liquid chromatography coupled with mass spectrometry.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026