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

A

Assiut University

Status

Unknown

Conditions

Bilateral Superficial Cervical Block

Treatments

Drug: Dexamethasone
Device: ultrasound
Drug: bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT03109691
01003060468

Details and patient eligibility

About

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

Enrollment

60 estimated patients

Sex

All

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

group 1
Active Comparator group
Description:
30 patients will receive bupivacaine
Treatment:
Device: ultrasound
Drug: bupivacaine
Drug: Dexamethasone
group 2
Active Comparator group
Description:
30 patients will receive bupivacaine and Dexamethasone. .
Treatment:
Device: ultrasound
Drug: bupivacaine

Trial contacts and locations

1

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Central trial contact

mohmed Bakri, prof

Data sourced from clinicaltrials.gov

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