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Looking for Minimum Dose to Induce Sympathectomy in Infraclavicular Brachial Plexus Block

Looking for Minimum Dose to Induce Sympathectomy in Infraclavicular Brachial Plexus Block

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04417608
Enrollment
66
Registered
2020-06-04
Start date
2020-06-04
Completion date
2021-07-04
Last updated
2020-06-04

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

Conditions

Finding the Minimum Dose to Induce Sympathectomy in Infraclavicular

Brief summary

For patients who undergoing hemodialysis, it is important to have good AV fistula. One third of AV fistula usually fail during early stage. It is helpful to use nerve block to dilate the blood vessels and enhance the prognosis. But 0.2% Ropivacaine usually cause muscle weakness in present studies. The investigators hope to find the lowest concentration to provide sympathectomy without muscle weakness. Because the patients with hemodialysis usually have multiple co-morbidity, thus we choose patients with forearm fracture at the first place. With this result, the investigators can design further study for patients with hemodialysis. The investigators prefer proximal approach because brachial plexus run together in the cosctoclavicular space and show lower incidence of incomplete work.

Interventions

Ultrasound-guided infraclavicular brachial plexus block

Sponsors

Taipei Medical University WanFang Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age between 20-80 y/o, BW: 40-90 kilograms,ASA class I-III,No pre-existing neuropathy,Scheduled for upper limb surgery.

Exclusion criteria

1. Pre-existing neuropathy (ex: polyneuropathy) 2. History of allergy to xylocaine、ropivacaine、epinephrine 3. Emergent surgery 4. Coagulopathy 5. Patient who can not express themselves

Design outcomes

Primary

MeasureTime frameDescription
Change of diameter of basilic vein and brachial arteryChange from baseline diameter(pre-nerve block) at 45minUse ultrasound to measure the difference of diameter at different time point.

Secondary

MeasureTime frameDescription
Sensory block of upper limb45min post nerve blockA validated 3-point scale was used: 0 = no block (patient has normal sensation), 1 = patient can feel cold, but the sensation is reduced compared with the unblocked side, and 2 = complete anesthesia.
Motor block of upper limb45min post nerve blockA validated 3-point scale was used: 0 = no block (patient has normal power), 1 = patient can feel weakness with the unblocked side, and 2 = complete anesthesia.

Outcome results

None listed

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