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Clinical Trial Summary

The investigators included prospectively 35 patients undergoing an intermediate cervical block under ultrasound (GP1) before a thyroidectomy ,compared to a group of 35 patients without a block (GP2).


Clinical Trial Description

The investigators performed prospective trial with 70 patients randomized in two groups each of 35:

- Group 1 (GP1): bilateral echo-guided intermediate cervical plexus bloc (ICB) by 10 ml of isobaric Bupivacaine (0.25%).

- Group 2 (GP2): control.

Ten minutes after ICB, general anesthesia was realised. Total dose of Remifentanil is calculated upon awakening, the postoperative pain is determined by visual analog scale from 0 to 10 (VAS) statements to H0, H2, H4, H6, H12 and H24. Whenever VAS is greater than or equal to 4, a morphine titration was administered.

Total dose consumption, side effects and satisfaction are noted at the end of protocol. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03107585
Study type Interventional
Source University Hospital, Mahdia
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date January 2016

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