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Ultrasound-guided Intermediate Cervical Plexus Block for Carotid Surgery

I

Institut Mutualiste Montsouris

Status

Completed

Conditions

Carotid Artery Stenosis

Treatments

Procedure: Ultrasound-guided intermediate cervical plexus block

Study type

Observational

Funder types

Other

Identifiers

NCT02450734
IMM CEPAR : 2012-014

Details and patient eligibility

About

Since stroke and myocardial ischemia are major causes of perioperative morbidity and mortality associated with carotid endarterectomy, monitoring the brain and ensuring the best hemodynamic stability are important goals of perioperative management.

The investigators conducted a prospective observational study about efficacy and safety of the ultrasound-guided intermediate cervical plexus block (CPB), with early (immediate postoperative) and mid-term (day 30) outcomes in awake patients undergoing carotid endarterectomy.

Full description

From April 2011 to May 2013, all patients undergoing a carotid endarterectomy were informed of the study and prospectively included. The study was approved by our institutional ethical Review Board (CEPAR, Institut Mutualiste Montsouris Paris France). Oral consent was obtained from patients. Written informed consent of the patients to participate was not necessary according to the French law regarding observational study.

The anesthesiologist in charge of the patient recorded all the parameters of the ultrasound-guided intermediate cervical plexus block: facility and duration of block performance, local anesthetic volume, quality of anesthesia and surgical dissection, and adverse effects of the intermediate CPB. . Neurological status was assessed intraoperatively, in the postoperative setting and at one month after the procedure. Perioperative hemodynamic stability (intraoperative non invasive blood pressure variations) and pulse oxymetry were recorded. As well as ECG and cardiac Troponin I (cTnI) measurments performed the day before surgery and each morning during the 3 first postoperative days. Any clinical coronary or neurological event was recorded at one month.

Statistical analysis was performed on Prism 6 for Mac OS X (Version 6.0c, www.graphpad.com). Data are presented as mean ± standard deviation (SD) for continuous data and number (percentage) for categorical data.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing carotid endarterectomy

Exclusion criteria

  • None

Trial design

50 participants in 1 patient group

Carotid endarterectomy
Description:
Realisation of an ultrasound-guided intermediate cervical plexus block for anesthesia of carotid endarterectomy
Treatment:
Procedure: Ultrasound-guided intermediate cervical plexus block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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