Effective Postoperative Pain Treatment After Sternotomy. Comparison of the Erector Spinae Plane Block vs Conventional Opioid Treatment

Pain Reliefe Clinical Trial

— VUSCH/POPT1  

Official title:

VUSCH/PostOperativePainTreatment1

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03915301
• Other study ID #: 1/2019/VUSCH/EK
• Status: Recruiting
• Start date: July 20, 2020
• Est. completion date: December 31, 2020

Study information

• Verified date: July 2019
• Source: Pavol Jozef Safarik University
• Contact: Ladislav Kocan, MD, PhD
• Phone: 00421907440250
• Email: lkocan[@]vusch.sk
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Comparison of effect between Erector Spinae plane block and conventional opioid treatment after cardiac surgery

Description:

Comparison of effect between Erector Spinae plane block and conventional opioid treatment after cardiac surgery. In group "A" will be erector spinae plane block provided in the thoracic part of the body, under ultrasound control. In the group B will be analgesia provided by Pethidine. Numerical pain score will be recorded every 2 hours, also usage of analgetics will be recorded in both groups.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 31, 2020
• Est. primary completion date: November 1, 2020
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

• Postoperative state after cardiac surgery, Serious pain NRS 8-10

Exclusion Criteria:

• disagreement

Related Conditions & MeSH terms

• Pain Reliefe

Intervention

Procedure:
• Satisfaction assessed by the VAS [followed by its scale information in the Description]
Erector spinae plane block provided in thoracic part of spine, VAS scale 0-10

Locations

Country	Name	City	State
Slovakia	East Slovak Institute for Cardiovascular Diseases	Kosice

Sponsors (1)

Lead Sponsor	Collaborator
Pavol Jozef Safarik University

Country where clinical trial is conducted

Slovakia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Satisfaction with pain treatment assessed by the numerical rating scale VAS	Pain assessed by VAS 0-10 score	12 hours