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Not Yet Recruiting NCT05729308

Comparative Study Between Caudal Epidural Block and Bilateral Erector Spinae Plane Block in Lumbosacral Spine Surgeries.

Conditions: Postoperative Pain, Acute

Sex: All
Ages: 18 Years – 65 Years
Phase: NA
Enrollment: 78
Sponsor: Ain Shams University

Location: Egypt

Summary

It is widely believed that major lumbosacral spine surgeries are associated with severe postoperative pain that may delay the functional recovery of the patient. Caudal epidural injection (CE) has an important role in providing effective pain relief post lumbosacral spine surgeries by blocking sensory input at the level of the spinal cord. Erector Spinae Plane Block (ESPB) is a relatively new technique of trunk fascial block which was introduced in 2016. Reports showed that ESPB significantly relieved postoperative pain in patients with lumbosacral spine surgery, reducing the use of analgesics.The overall benefit of intravenous (IV) analgesia versus pre-emptive analgesia by caudal epidural or erector spinae block is still controversial.The aim of this study is to compare the pre-emptive analgesic effect of bilateral erector spinae plane block versus Caudal epidural analgesia versus the conventional intravenous analgesia in adult patients undergoing lumbosacral spine surgeries under general anesthesia.

Eligibility Criteria

Inclusion Criteria:Patients scheduled for lumbosacral spine surgery level from L4 to S1.American Society of Anesthesiologists classification (ASA) class I or II.Exclusion Criteria:Refusal of procedure or participation in the study.American Society of Anesthesiologists classification (ASA) class III or IV.Coagulation disorders (platelets count < 100,000; International normalized ratio >1.4; Patient control time< 60%) and coagulopathies.Skin lesion or infection at the injection site.Known allergy to any of the medications used.Chronic opioid users.Patients with pre-operative opioid consumption

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05729308). StuddyBuddy aggregates publicly available trial information.