Status:
RECRUITING
Analgesic Efficacy of Erector Spinae Plane Block vs External Oblique Intercostal Plane Block in Subcostal Cancer Surgeries
Lead Sponsor:
National Cancer Institute, Egypt
Conditions:
Analgesia
Erector Spinae Plane Block
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
This study aims to evaluate the impact of ultrasound-guided erector spinae plane block compared to ultrasound-guided external oblique intercostal plane block regarding management of postoperative acut...
Detailed Description
Subcostal incisions in cancer surgeries as in hepatectomy and nephrectomy are a cause of severe pain and can lead to significant respiratory impairment. Regional anesthesia of the trunk and abdominal ...
Eligibility Criteria
Inclusion
- Age (18-65) Years.
- Both sexes.
- Body mass index (BMI): (20-40) kg/m2.
- American Society of Anesthesiology (ASA) physical status II, III.
- Type of surgery; unilateral subcostal incision in hepatectomy and nephrectomy.
Exclusion
- Patient refusal.
- Subcostal incisions that are crossing the midline or midline incision.
- Age \<18 years or \>65 years
- BMI \<20 kg/m2 and \>40 kg/m2
- Known sensitivity or contraindication to drugs used in the study
- Contraindication to regional anesthesia e.g. local infection at the site of introduction, pre-existing peripheral neuropathies, and coagulopathy.
- Pregnancy.
- Physical status ASA IV
- patients on chronic analgesic therapy (daily morphine ≥30 mg or equivalent dose of other opioids or tramadol or any medication for neuropathic pain)
- patients with a history of drug abuse
- patients with neuropsychiatric diseases; patients with a history of chronic pain syndromes that may enhance sensitivity to pain, for example, fibromyalgia
- All patients who are going to have severe intra- or post-operative bleeding or will require postoperative mechanical ventilation are also excluded from the study.
Key Trial Info
Start Date :
July 25 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 27 2025
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT06519708
Start Date
July 25 2024
End Date
May 27 2025
Last Update
July 26 2024
Active Locations (1)
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1
Cairo University
Cairo, Egypt, 11796