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

Aydin Adnan Menderes University

Status: Unknown

Conditions: Cardiac Surgery; Erector Spinae Plane Block

Treatments: Procedure: erector spinae plane block; Drug: iv analgesia

Study type: Interventional

Funder types: Other

Identifiers

NCT04420104

AMU

Details and patient eligibility

About

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

Full 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.

Enrollment: 40 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Must be ASA score I-III
• Must be 18-75 years old
• must undergo cardiac surgery

Exclusion criteria

• emergency surgery,
• bleeding diathesis,
• presence of contraindications to LA agents used in this study,
• use of chronic opioids,
• psychiatric disorders.
• prolonged extubation
• presence of infection at the injection site.
• cardiovascular conditions (EF<40, LMCA obstruction)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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40 participants in 2 patient groups

esp block group

Experimental group

Treatment:

Procedure: erector spinae plane block

Drug: iv analgesia

control group

Active Comparator group

Treatment:

Drug: iv analgesia