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NCT04554186 Clinical Trial

Serratus Anterior Plane Block Versus Thoracic Paravertebral Block.

Analgesia Clinical Trial

Official title:
Ultrasound Guided Serratus Anterior Plane Block Versus Thoracic Paravertebral Block in Emergency Department Rib Fracture

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04554186
Other study ID # 112-11/2018
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 22, 2020
Est. completion date January 15, 2021

Study information
Verified date September 2020
Source Minia University
Contact Ahmed G Shehata, Master
Phone 1067622270
Email ahmedgamalicu@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare between serratus anterior plane block and thoracic Paravertebral block in analgesia for patients with multiple rib fractures

Description:

The study will be conducted in a prospective randomised controlled. Patients will be allocated into three groups

Control group:

The patient will receive fentanyl patch 50 microgram

TPVB group:

The patient will receive thoracic vertebral plane lock 0.4ml/kg bupivacaine 0.1 25% will be administered. For continuous infusion catheter will be inserted . Then a rate of 7ml / hour to max 10 ml / hour of bupivacaine 0.0625%

SAPB group,:

Patient will receive serratus anterior plane block 0.4ml / kg bupivacaine 0.125% will be injected to open the space then a catheter will be advanced For continuous infusion of 0.0625 % bupivacaine at 7 ml / hour

Recruitment information / eligibility
Status Recruiting
Enrollment 60
Est. completion date January 15, 2021
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- ASA 1_3 Age 18_60 Unilateral fracture ribs

Exclusion Criteria:

- Drug allergy Morbid obese Opioid dependence Patients refuse

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Serratus anterior plane block
Injection of bupivacaine between serratus anterior plane and latissimus dorsi muscle using ultrasound
• Thoracic Paravertebral block
Injection of bupivacaine in the thoracic Paravertebral space using ultrasound
• Control
Place a fentanyl patch 50 microgram

Locations
Country Name City State
Egypt Minia university hospital Minya

Sponsors (1)
Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary VAS score Visual analogue pain score describe by the patient 24 hour
Secondary Total analgesic consumption Total opioid consume by the patient in 24 hour 24 hour
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