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Erector Spinae Plane Block for Postoperative Pain Management

K

Kahramanmaraş Sütçü İmam University (KSU)

Status

Completed

Conditions

Pain
Post Operative Pain

Treatments

Procedure: Erector spinae plane block
Procedure: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT05697315
2021-02-03

Details and patient eligibility

About

Erector spinae plane (ESP) block is an interfacial plane block with visceral and somatic analgesic activity at paraspinal muscles. This study aims to examine the postoperative analgesic efficacy of ESP block after cesarean section (CS) with Pfannenstiel incision under spinal anesthesia.

Full description

The study included 54 patients with mild systemic disease (ASA II patients) who would undergo elective CS under spinal anesthesia. They were randomly divided into an ESP block group (Group E) and a control group (Group C). After the surgery, Group E patients underwent ultrasound-guided bilateral ESP block with 20 ml of 0.25% bupivacaine at the lateral decubitus position, while Group C received no intervention. Patients in both groups received parenteral patient-controlled analgesia. The patients' post-operative 24-hour opioid consumption, regular Visual Analogue Scale (VAS) measurements, and need for rescue analgesics were evaluated. Statistical analysis was performed using SPSS 21 program. Demographic and other data were assessed using independent samples t-test, Mann-Whitney U test, and Chi-square analysis.

Enrollment

56 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ASA II patients
  • 18-45 years who underwent CS with Pfannenstiel incision under spinal anesthesia
  • agreed to participate in the study

Exclusion criteria

  • Patients with infection at the injection site
  • Coagulopathy Allergy to amide-type local anesthetics
  • History of peripheral neuropathy
  • Hepatic and/or renal failure
  • Refusing the procedure
  • patients with heart disease

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

56 participants in 2 patient groups

Control group
Sham Comparator group
Description:
No block was performed, tramadol was administered with patient-controlled analgesia (PCA) and all patients were followed in the ward.
Treatment:
Procedure: Control
Erector spinae plane block
Active Comparator group
Description:
Erector spinae plane block was performed, tramadol was administered with patient-controlled analgesia (PCA) and all patients were followed in the ward.
Treatment:
Procedure: Erector spinae plane block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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