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Inferior Vena Cava (IVC) Diameters Before & After Interscalene Block

University of California San Diego logo

University of California San Diego

Status

Withdrawn

Conditions

IVC - Inferior Vena Cava Abnormality

Treatments

Procedure: Interscalene Brachial Plexus Block

Study type

Observational

Funder types

Other

Identifiers

NCT03989076
UCSD 181482

Details and patient eligibility

About

The purpose of this study is to understand how changes to breathing patterns in the chest affect blood flow to the heart from the inferior vena cava in the abdomen. Ultrasound of the upper abdomen will be used to visualize changes in breathing patterns in the chest and blood flow in the abdomen.

Full description

In recent practice, point-of-care ultrasound has been used to assess the size and respiratory variation of the inferior vena cava as a marker for volume status and fluid responsiveness. Little investigation has occurred regarding the mechanism of observed respiratory variation. Anesthetic plans for surgery (e.g. shoulder replacement) frequently employ interscalene injections to target and block the brachial plexus, which (on the same side) results in phrenic nerve palsy and paralysis of the diaphragm. The goal of this study is to examine the relationship between diaphragmatic function and variation in IVC diameter. Specifically, the investigators will evaluate and compare the size and variability of the inferior vena cava by point-of-care ultrasound before and after brachial plexus block.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adult (age > 18 years)
  • Scheduled to receive an interscalene block

Exclusion criteria

  • Any person with known, pre-existing phrenic nerve, diaphragmatic, or inferior vena cava anomaly.
  • Patients who cannot be successfully imaged by ultrasound or who cannot participate in spirometry will additionally be excluded.
  • Non-English speaking patients will be excluded as well as there is no research funding to translate consent forms. Given that there is no potential benefit to participation in the study, this does not exclude these individuals from any potentially beneficial therapy.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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