Faculty of 1000 evaluation for Randomized clinical trial of intraoperative superficial cervical plexus block versus incisional local anaesthesia in thyroid and parathyroid surgery.

2014 ◽  
Author(s):  
Mario Salvi
Keyword(s):  
Clinical Trial ◽  
Randomized Clinical Trial ◽  
Local Anaesthesia ◽  
Parathyroid Surgery ◽  
Cervical Plexus ◽  
Superficial Cervical Plexus Block ◽  
Cervical Plexus Block ◽  
Plexus Block

Randomized clinical trial of intraoperative superficial cervical plexus blockversusincisional local anaesthesia in thyroid and parathyroid surgery

2013 ◽  
Vol 100 (13) ◽  
pp. 1732-1738 ◽  
Author(s):  
R. J. Egan ◽  
J. C. Hopkins ◽  
A. J. Beamish ◽  
R. Shah ◽  
A. G. Edwards ◽  
...  
Keyword(s):  
Clinical Trial ◽  
Randomized Clinical Trial ◽  
Local Anaesthesia ◽  
Parathyroid Surgery ◽  
Cervical Plexus

scholarly journals Ultrasound-guided superficial cervical plexus block for analgesia in patients undergoing craniotomy via suboccipital retrosigmoid approach: study protocol of a randomised controlled trial

BMJ Open ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. e034003
Author(s):  
Kun Peng ◽  
Min Zeng ◽  
Jia Dong ◽  
Xiang Yan ◽  
Dexiang Wang ◽  
...  
Keyword(s):  
Nerve Block ◽  
Rating Scale ◽  
Numerical Rating Scale ◽  
Controlled Trial ◽  
Control Group ◽  
Cervical Plexus ◽  
Ethics Review ◽  
Superficial Cervical Plexus Block ◽  
Cervical Plexus Block ◽  
Plexus Block

IntroductionScalp nerve block has been proven to be an alternative choice to opioids in multimodal analgesia. However, for the infratentorial space-occupying craniotomy, especially the suboccipital retrosigmoid craniotomy, scalp nerve block is insufficient.Methods and analysisThe study is a prospective, single-centre, randomised, paralleled-group controlled trial. Patients scheduled to receive elective suboccipital retrosigmoid craniotomy will be randomly assigned to the superficial cervical plexus block group or the control group. After anaesthesia induction, superficial cervical plexus nerve block will be performed under the guidance of ultrasound. The primary outcome is the cumulative consumption of sufentanil by the patient-controlled intravenous analgesia pump within 24 hours after surgery. Secondary outcomes include the cumulative consumption of sufentanil at other four time points and numerical rating scale pain severity score.Ethics and disseminationThe protocol (version number: 2.0, 10 April 2019) has been approved by the Ethics Review Committee of China Registered Clinical Trials (Ethics Review No. ChiECRCT-20190047). The findings of this study will be disseminated in peer-reviewed journals and at scientific conferences.Trial registration numberNCT04036812

Does Bilateral Superficial Cervical Plexus Block Decrease Analgesic Requirement After Thyroid Surgery?

2006 ◽  
Vol 102 (4) ◽  
pp. 1174-1176 ◽  
Author(s):  
Zeynep Eti ◽  
Pnar Irmak ◽  
Bahadr M. Gulluoglu ◽  
Manuk N. Manukyan ◽  
F Ylmaz Gogus
Keyword(s):  
Thyroid Surgery ◽  
Cervical Plexus ◽  
Analgesic Requirement ◽  
Superficial Cervical Plexus Block ◽  
Cervical Plexus Block ◽  
Plexus Block
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