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Comparison of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block

D

Diskapi Yildirim Beyazit Training and Research Hospital

Status

Completed

Conditions

Postoperative Pain
Erector Spinae Plane Block
Breast Neoplasms
Serratus Posterior Superior Intercostal Plane Block
Acute Pain

Treatments

Procedure: Serratus Posterior Superior Intercostal Plane Block
Procedure: Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT06407037
AEŞH-EK1-2023-824

Details and patient eligibility

About

Breast cancer is the most common malignancy in women. Modified radical mastectomy, a surgical procedure in the treatment of breast cancer, is one of the standard treatments. Postoperative pain can seriously reduce the quality of life in patients, and inadequately treated acute pain can trigger chronic pain syndrome. Therefore, thoracic paravertebral block and thoracic epidural block are effective in postoperative analgesia. However, the use of these blocks is limited due to complications. In recent years, less invasive blocks, such as pectoral nerve block (PECS I-II), Serratus anterior plane block (SAPB), Erector spinae plane block (ESPB), and Serratus Posterior Superior intercostal Plane Block (SPSİPB) have been applied. In this study, it was aimed to compare the analgesic effectiveness of ESPB and SPSİPB applications in patients undergoing breast surgery.

Full description

Postoperative pain will be assessed during resting and coughing with a visual analog scale (0-10 cm) and nausea and vomiting with a Postoperative Nausea Vomiting Score at the postoperative 1, 4, 8, 12, and 24 hours. The amount of tramadol consumed in the postoperative period will be recorded. Patient satisfaction will be assessed with the Likert scale at postoperative 24 hours.

Enrollment

50 patients

Sex

Female

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Those aged 18-65
  • Those with ASA scores I-II-III
  • Those with a body mass index (BMI) between 18-35
  • Patients who will undergo breast surgery

Exclusion criteria

  • Those under the age of 18 and over the age of 65
  • Those with ASA score IV and above
  • Those with a history of allergy to the drugs to be blocked
  • Those with a history of bleeding diathesis
  • Patients with infection in the area to be blocked
  • Those with a BMI below 18 and above 35
  • Patients who underwent surgery under emergency conditions

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

50 participants in 2 patient groups

Erector Spinae Plane Block
Active Comparator group
Description:
Following the visualization of the anatomical structures, the nerve block needle was advanced via the in-plane technique beneath the erector spinae muscles until the interfascial space was reached. After hydrodissection with 2 ml normal saline, 30 ml of 0.25% bupivacaine was injected into the area.
Treatment:
Procedure: Erector Spinae Plane Block
Serratus Posterior Superior Intercostal Plane Block
Active Comparator group
Description:
The probe was placed on the spinae scapula in the sagittal plane to identify the second and third ribs. The trapezius, rhomboid, serratus posterior superior muscle were visualized. The needle was inserted just above the third rib deeply into the serratus posterior superior muscle. Two mL isotonic was administrated for the correction. Then, 30 mL of 0.25% bupivacaine was administrated between serratus posterior superior muscle and rib.
Treatment:
Procedure: Serratus Posterior Superior Intercostal Plane Block

Trial contacts and locations

1

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Central trial contact

Musa Zengin, Associate Professor; Emine Arık, Associate Professor

Data sourced from clinicaltrials.gov

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