Ultrasound Guided Bilateral Superficial Cervical Block for Post-operative Pain Therapy in Thyroid Surgery

Bilateral Superficial Cervical Block Clinical Trial

Official title:

Dexamethasone Effect Using Ultrasound Guided Bilateral Superficial Cervical Block for Postoperative Pain Therapy in Thyroid Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03109691
• Other study ID #: 01003060468
• Status: Recruiting
• Phase: N/A
• Start date: January 28, 2018
• Est. completion date: September 2020

Study information

• Verified date: June 2019
• Source: Assiut University
• Contact: mohmed Bakri, prof
• Phone: +20882413201
• Email: mhbakri[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ultrasound Guided Bilateral Superficial Cervical Block for Postoperative Pain Therapy in Thyroid Surgery

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: September 2020
• Est. primary completion date: July 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 50 Years

Eligibility

Inclusion Criteria:

• American Society of Anesthesiologists (ASA) class I and II

Exclusion Criteria:

• allergy to local anesthetics, bleeding diatheses, and local infection or sepsis thyrotoxicosis and , malignancy.

Related Conditions & MeSH terms

• Bilateral Superficial Cervical Block

Intervention

Drug:
• bupivacaine
group 1
• Dexamethasone
group 2

Device:
• ultrasound
in all groups

Locations

Country	Name	City	State
Egypt	Assiut University Hospital	Assiut

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Analog Scale	visual analoge scale (VAS)	through first 24 h postoperative.
Secondary	HEART RATE	heart rate( beats per minute)	5,10,15,30,60,90,120 min introperative
Secondary	postoperative nausea, vomiting	postoperative nausea, vomiting was recorded	through first 24h postoperative
Secondary	The time period for the first analgesic requirement	total dose	through first 24h postoperative
Secondary	blood pressure	blood pressure (mm Hg)	5,10,15,30,60,90,120 min intraoperative