Clinical Trial

Perfusion Index in Caudal Epidural Anasthesia

Not Yet Recruiting Phase 4
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Record status
This record was last updated November 19, 2024 (before its estimated February 2026 completion). Its status may not reflect the trial's current state.
Summary
A caudal epidural block is among the most widely administered techniques of regional anesthesia in pediatric patients. It helps in reducing the intraoperative dose of inhalational anesthetic agent used for maintenance of anesthesia and in addition provides an excellent postoperative analgesia without the side effects of intravenous opioid medication, like nausea and vomiting during emergence, cardiovascular, and respiratory depression. the aim of the study was to assess, perfusion index (PI) as an indicator for success of caudal block onset in pediatric patients scheduled for elective surgery of lower abdomen, pelvic region, genital region, or lower limbs. with guidance of ultrasonography.
Trial Details
NCT Number NCT06695520
Lead Sponsor Assiut University
Conditions Caudal Epidural Block
Enrollment 54 participants
Start Date 2024-12-01
Primary Completion 2026-02 (estimated)
Study Completion 2026-03 (estimated)
Updated on ClinicalTrials.gov 2024-11-19