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

Not Applicable
Conditions
Bilateral Superficial Cervical Block
Interventions
Registration Number
NCT03109691
Lead Sponsor
Assiut University
Brief Summary

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

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
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.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
group 1ultrasound30 patients will receive bupivacaine
group 2ultrasound30 patients will receive bupivacaine and Dexamethasone. .
group 1Dexamethasone30 patients will receive bupivacaine
group 1bupivacaine30 patients will receive bupivacaine
group 2bupivacaine30 patients will receive bupivacaine and Dexamethasone. .
Primary Outcome Measures
NameTimeMethod
Visual Analog Scalethrough first 24 h postoperative.

visual analoge scale (VAS)

Secondary Outcome Measures
NameTimeMethod
blood pressure5,10,15,30,60,90,120 min intraoperative

blood pressure (mm Hg)

postoperative nausea, vomitingthrough first 24h postoperative

postoperative nausea, vomiting was recorded

The time period for the first analgesic requirementthrough first 24h postoperative

total dose

HEART RATE5,10,15,30,60,90,120 min introperative

heart rate( beats per minute)

Trial Locations

Locations (1)

Assiut University Hospital

🇪🇬

Assiut, Egypt

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