Erector spinae plane block: Patients will receive an ultrasound-guided erector spinae plane block.
Study summary
This study aims to evaluate the efficacy of the erector spinae plane block (ESPB) on postoperative analgesia in patients undergoing laparoscopic abdominal surgeries.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥ 18 years.
* Both sexes.
* American Society of Anesthesiologists (ASA) physical status I-II.
* Body mass index (BMI) between 20-30 kg/m2.
* Patients undergoing laparoscopic abdominal surgeries under general anesthesia.
Exclusion Criteria:
* Bleeding or coagulation disorders.
* Having local sepsis, pre-existing.
* Peripheral neuropathies.
* Chronic pain conditions.
* Having any contraindication to regional anesthesia administration.
* Opioid dependency.
* Hypertension.
* Uncontrolled diabetes mellitus.
Primary outcome measure(s)
Time to the 1st rescue analgesia — 24 hours postoperatively Time to the first request for the rescue analgesia (time from the end of surgery to first dose of morphine administrated).
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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