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Ultrasound Guided Intermediate Cervical Plexus Block and Additional Perivascular Local Anesthetic Infiltration

NCT02336958 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2015-03-23

Study results available
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Summary

For ultrasound guided intermediate cervical plexus block this randomized comparison is testing the hypothesis, that an additional perivascular infiltration is associated with increased block quality.

Conditions

  • Carotid Stenosis

Interventions

DRUG

intermediate cervical plexus block ropivacaine

20ml ultrasound guided intermediate cervical plexus block.

DRUG

pericarotidal infiltration (active comparator) ropivacaine

5ml ropivacaine 0.75% (active comparator): pericarotidal infiltration.

DRUG

jugular infiltration prilocaine

5ml prilocaine 1% jugular infiltration for wound drainage.

DRUG

pericarotidal infiltration (placebo comparator) saline

5ml saline 0.9% (placebo comparator): pericarotidal infiltration.

Sponsors & Collaborators

  • Helios Research Center

    lead OTHER

Principal Investigators

  • Ronald Seidel, Dr.med. · Helios Kliniken Schwerin, Klinik für Anästhesiologie und Intensivtherapie, Wismarsche Strasse 393-7, 19049 Schwerin, Germany

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-12-31
Completion
2014-12-31

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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 NCT02336958 on ClinicalTrials.gov