Bilateral Erector Spinae Plane Block in Paediateric Cardiac Surgery

Pain Management Clinical Trial

Official title:

Bilateral Erector Spinae Plane Block in Paediateric Cardiac Surgery, Randomized Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04168177
• Other study ID #: ASDF
• Status: Recruiting
• Phase: N/A
• Start date: February 17, 2019
• Est. completion date: December 20, 2020

Study information

• Verified date: June 2020
• Source: Assiut University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ultrasound guided erector spinae plane block will be done for childern under going midline sternotomy for cardiac surgery. It is a novel block which is suspected to give powerful analgesia, decrease anaesthetic consumption and decrease awareness on cardiac bypass

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 20, 2020
• Est. primary completion date: July 17, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years to 12 Years

Eligibility

Inclusion Criteria:

• elective surgery

• childern between 4 and 10 years

Exclusion Criteria:

• emergency

• infection at injection site

• allergy to local anaestheics

Related Conditions & MeSH terms

• Pain Management

Intervention

Procedure:
• PCA
Patient controlled analgesia
• ESP
erector spinae plane block

Locations

Country	Name	City	State
Egypt	Assiut university	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 analogue score	pain scores will be assessed by anaesthesia and ICU nurse. zero mean no pain an 10 indicate the worst pain.	48 hours
Secondary	intraoperative anaesthetic consumption		6 hours