Comparison of Postoperative Analgesic Consumption of the Erector Spina Plane Block and Serratus Anterior Plane Block

TC Erciyes University

Status: Unknown

Conditions: Thoracic Diseases

Treatments: Procedure: Erector Spinae Plane block ( Group ı); Procedure: Control Group (GROUPIII); Procedure: Serratus Anterior Plane block ( Group ıı)

Study type: Interventional

Funder types: Other

Identifiers

NCT03904082

2019/175

Details and patient eligibility

About

To evaluate the ability of Erector spina Plane block and Serratus Anterior Plane block to decrease postoperative pain and analgesia requirements in patients undergoing thoracotomy.

Full description

Thoracic wall nerve blocks such as Erector spina Plane block and Serratus Anterior Plane block have become popular for preoperative pain control in patients undergoing thoracotomy.

Enrollment: 105 estimated patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

ASA I- ASA II Patients

Exclusion criteria

• history of allergy to the study medication
• refusal to participate

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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105 participants in 3 patient groups, including a placebo group

Erector spinae plane block group (ESP)

Active Comparator group

Description:

Single- shot ultrasound (Esaote Mylab30) guided ESP block with 15 ml 0.25% bupivacain (Marcain 0.5%, Astra Zeneca, Turkey) at the T4 vertebral level will performed preoperatively to patients in the ESP group (Group I).

Treatment:

Procedure: Erector Spinae Plane block ( Group ı)

Serratus Anterior Plane Block Group (SAP)

Active Comparator group

Description:

Single- shot ultrasound (Esaote Mylab30 )guided SAP block with 15 ml 0.25% bupivacain (Marcain 0.5%, Astra Zeneca, Turkey) the T4 vertebral level will performed preoperatively to patients in the SAP group( Group II).

Treatment:

Procedure: Serratus Anterior Plane block ( Group ıı)

Control Group

Placebo Comparator group

Description:

The Control group receive no intervetion ( Group III).

Treatment:

Procedure: Control Group (GROUPIII)