Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID07232940

Comparison of Ultrasound-Guided Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block for Pain Relief After Video-Assisted Thoracoscopic Surgery

Led by Bursa City Hospital · Updated on 2025-12-16

90

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

B

Bursa City Hospital

Lead Sponsor

U

Ulusoy, Emre, M.D.

Collaborating Sponsor

AI-Summary

What this Trial Is About

Video-assisted thoracoscopic surgery (VATS) is a minimally invasive procedure using small chest incisions, but patients often experience significant postoperative pain due to tissue and rib trauma. Poorly controlled pain can lead to chronic issues, so effective pain relief is crucial. This study compares two types of nerve blocks, erector spinae plane block (ESPB) and the newer serratus posterior superior intercostal plane block (SPSIPB), to evaluate their effectiveness and patient satisfaction in managing pain after VATS. Participants will receive either the ESPB or SPSIPB nerve block during surgery. Both involve using ultrasound guidance to inject a local anesthetic containing bupivacaine and epinephrine near specific muscles and nerves in the back or upper chest area. The SPSIPB targets nerves between the C3 and T10 spinal levels, while the ESPB targets the T5 level. This comparison aims to determine which block provides better pain control after VATS. During the study, opioid use will be measured at multiple times within the first 24 hours after surgery to assess pain control. Pain scores will be recorded using a numerical scale, and patient recovery quality will be evaluated 24 hours post-surgery. Additional assessments include pain inventories and anxiety/depression scales at three months after surgery. Participants will be monitored closely throughout the study period, which runs until May 2026.

CONDITIONS

Brief Title

ESP vs SPSIP Block in VATS Analgesia

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 65 years
  • ASA physical status I to III
  • Scheduled for elective video-assisted thoracoscopic surgery (VATS)
Not Eligible

You will not qualify if you...

  • Patients who do not consent to participate
  • Patients with coagulopathy
  • History of local anesthetic allergy or toxicity
  • Hepatic or renal failure
  • Uncontrolled diabetes
  • Uncontrolled hypertension
  • Mentally disabled patients
  • Chronic pain treatment with opioids
  • Use of antidepressant medication
  • Neuropathic pain
  • Infection at the injection site
  • Pregnant or breastfeeding women, or suspected pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 24 hours post-surgery

Participants undergo video-assisted thoracoscopic surgery (VATS) and receive either an erector spinae plane block (ESPB) or serratus posterior superior intercostal plane block (SPSIPB) for postoperative pain relief.

1 surgical visit and assessments at 0, 2, 4, 8, 16, and 24 hours post-surgery

Follow-up

Duration - 3 months

Participants are assessed for pain, recovery, and psychological status after surgery, including evaluations at 3 months postoperatively.

1 follow-up visit at 3 months post-surgery

Trial Site Locations

Total: 1 location

1

Bursa City Hospital

Bursa, Nilüfer, Turkey (Türkiye), 16110

Actively Recruiting

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Research Team

E

Eralp Çevikkalp

E

Emre ULUSOY

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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