Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT05810571

Comparison of Postoperative Analgesic Efficacy of the Erector Spina Plane Block and Quadratus Lumborum Block in Open Nephrectomy: a Prospective Randomized Clinical Study

Led by Kocaeli University · Updated on 2024-10-26

60

Participants Needed

2

Research Sites

114 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

patients who will undergo elective open nephrectomy will be divided into three groups; the control (PCA), the erector spina plane block, and the quadratus lumborum block. After standard anesthesia induction and monitorization then Bispectral index monitoring will be applied to all patients. Anesthesia will be maintained using sevoflurane in a mixture of oxygen and air. Continuous remifentanil infusion will be used for analgesia. Then patient's numeric rating scales and morphine pca consumptions will be recorded for one day.

CONDITIONS

Official Title

Comparison of Postoperative Analgesic Efficacy of the Erector Spina Plane Block and Quadratus Lumborum Block in Open Nephrectomy: a Prospective Randomized Clinical Study

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with ASA physical status 1 to 3
  • Elective open nephrectomy patients
  • Body mass index (BMI) less than 35
Not Eligible

You will not qualify if you...

  • Patients with ASA physical status 4, 5, or 6
  • Patients undergoing laparoscopic nephrectomy
  • Infection at the site of nerve block
  • Blood clotting disorders
  • Body mass index (BMI) greater than 35

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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2
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Trial Site Locations

Total: 2 locations

1

Kocaeli University Medical Faculty

İzmit, Turkey (Türkiye), 41100

Actively Recruiting

2

Kocaeli University Medical Faculty

Kocaeli, Turkey (Türkiye)

Active, Not Recruiting

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Research Team

Z

zehra ipek Arslan AYDIN, Professor

CONTACT

Z

Zehra ipek Arslan, Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

DIAGNOSTIC

Number of Arms

3

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