Comparation of Bilateral and Unilateral Erector Spinae Plane Block

Last updated: January 9, 2023
Sponsor: Ankara City Hospital Bilkent
Overall Status: Completed

Phase

N/A

Condition

Acute Pain

Pain

Anesthesia (Local)

Treatment

N/A

Clinical Study ID

NCT05152602
E2-21-228
  • Ages 18-60
  • All Genders

Study Summary

Although laparoscopic cholecystectomy is a minimally invasive surgery with many advantages, it is one of the operations with high postoperative pain scores. Opioids are frequently used to prevent postoperative pain. Due to the side effects of opioids, the amount of use is tried to be reduced. Regional anesthesia techniques can be used to minimize opioid consumption. Erector spina plane block was first described in 2016 by Forero et al. in the treatment of thoracic neuropathic pain. Since then, ESP block has been used as an anesthetic and analgesic technique. It is applied by injecting local anesthetic into the fascial plane located between the erector spina muscle and the transverse process of the vertebra. Several high-level studies have shown that the ESP block can be used to reduce postoperative pain after gastrointestinal surgery. Several studies have evaluated the effect of ESP block for pain relief after laparoscopic cholecystectomy. ESP block has been applied unilaterally or bilaterally in various studies. However, in the current studies in the literature, the advantages or disadvantages of the bilateral application of the ESP block compared to the unilateral application have not been evaluated. In this study, the investigators aimed to evaluate postoperative pain by applying ESP block to patients who underwent laparoscopic cholecystectomy and to evaluate the advantages of unilateral or bilateral application of ESP block over each other.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients who underwent laparoscopic cholecystectomy surgery between December 2021 andJanuary 2022 will participate in the study.

Exclusion

Exclusion Criteria:

  • There is no exclusion criteria for the study.

Study Design

Total Participants: 54
Study Start date:
January 01, 2022
Estimated Completion Date:
March 10, 2022

Connect with a study center

  • Ankara City Hospital

    Ankara, 06800
    Turkey

    Site Not Available

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