Clinical Trials Directory

Trials / Completed

CompletedNCT02450734

Ultrasound-guided Intermediate Cervical Plexus Block for Carotid Surgery

Safety and Efficiency of Ultrasound-guided Intermediate Cervical Plexus Block for Carotid Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
50 (actual)
Sponsor
Institut Mutualiste Montsouris · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREUltrasound-guided intermediate cervical plexus block

Timeline

Start date
2011-04-01
Primary completion
2013-05-01
Completion
2013-05-01
First posted
2015-05-21
Last updated
2015-05-21

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02450734. Inclusion in this directory is not an endorsement.