NCT04420104

Errector Spinae Plane Block for Postoperative Pain Management in Cardiac Surgery: A Randomized Controlled Trial

• Status: Unknown
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (estimated)
• Sponsor: Aydin Adnan Menderes University · Academic / Other
• Sex: All
• Age: 18 Years – 85 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to assess efficacy of erector spinae plane block (ESP) for postoperative pain management in cardiac surgery patients.

Detailed description

After being informed about the study and potential risks, all patients giving written informed consent will be randomised (single blind) as block group(patients is performed esp block) and control group. All patients will be evaluate during 48 hours for postoperative pain.

Conditions

• Erector Spinae Plane Block
• Cardiac Surgery

Interventions

Type	Name	Description
PROCEDURE	erector spinae plane block	ESP Block: Bilateral ESP block and with ultrasound guidance will be applied A total 40 ml, 20 ml bupivacaine 0.5%, 20 ml saline.
DRUG	iv analgesia	iv contromal

Timeline

• Start date: 2020-06-01
• Primary completion: 2021-01-01
• Completion: 2021-06-01
• First posted: 2020-06-09
• Last updated: 2020-07-08

Locations

1 site across 1 country: Turkey (Türkiye)