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Ultrasound-guided Intermediate Cervical Plexus Block

NCT02794974 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 29

Last updated 2018-12-19

Study results available
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Summary

The investigators test with the present study design, whether an ultrasound-guided blockade of the cervical plexus in combination with an additional application of local anesthetic to the superficial cervical ansa (facial nerve: cervical branch) leads to an improved quality of anesthesia.

Conditions

  • Internal Carotid Artery Stenosis

Interventions

OTHER

cervical plexus block

ultrasound-guided application of 20ml ropivacaine 0.75%

OTHER

facial nerve block

ultrasound-guided application of 5ml prilocaine 1%

OTHER

perivascular block

ultrasound-guided application of 5ml prilocaine 1%

Sponsors & Collaborators

  • Helios Research Center

    lead OTHER

Principal Investigators

  • Ronald Seidel, MD · Helios Medical Center Schwerin, Department of Anesthesiology and Intensive care,

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2017-08-31
Completion
2017-08-31

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02794974 on ClinicalTrials.gov