Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Abdominal Surgeries
NCT ID: NCT07272577
Last Updated: 2025-12-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
50 participants
INTERVENTIONAL
2025-12-10
2026-04-01
Brief Summary
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Detailed Description
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The role of ESPB as a better analgesic modality in reducing 24-hour opioid consumption has recently been established for post-operative analgesia in breast surgeries, video-assisted thoracoscopic surgery, and cardiothoracic surgeries.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Erector spinae plane block group
Patients will receive an ultrasound-guided erector spinae plane block.
Erector spinae plane block
Patients will receive an ultrasound-guided erector spinae plane block.
Control group
The block will not be performed, and the patients will be shifted to the operation room.
No interventions assigned to this group
Interventions
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Erector spinae plane block
Patients will receive an ultrasound-guided erector spinae plane block.
Eligibility Criteria
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Inclusion Criteria
* 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
* Having local sepsis, pre-existing.
* Peripheral neuropathies.
* Chronic pain conditions.
* Having any contraindication to regional anesthesia administration.
* Opioid dependency.
* Hypertension.
* Uncontrolled diabetes mellitus.
18 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Bahaa Gamal Saad Mohamed
Anesthesia and Intensive Care, Faculty of Medicine, Assiut University, Assiut, Egypt.
Locations
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Assiut University
Asyut, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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618
Identifier Type: -
Identifier Source: org_study_id
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