Postoperative Pain Clinical Trial
Official title:
A Randomized Controlled Trial of Sacral Erector Spinae Block Versus Caudal Block for Postoperative Analgesia After Hypospadias Surgery in Children
The purpose of this research study is to find the best way to decrease pain in children whom
have had hypospadias surgery. Investigators will perform two technique; Caudal block or
Sacral erector spinae block.
The results of this study will help learn how to best control pain in children having surgery
hypospadias surgery.
Children aged 1-9 years undergoing hypospadias surgeries would be recruited in this
randomized study.
Children would be monitored by electrocardiogram, pulse oximeter and non-invasive blood
pressure.
After preoxygenation for three minutes, anesthesia would be induced with 8% sevoflurane
inhalation in 50% oxygen and % 50 air ; 1ug/kg fentanyl and 3 mg/kg propofol is administered
intravenously. Then laryngeal mask is inserted when conditions are satisfactory (jaw relaxed,
lash reflex disappeared, no coughing, gagging, swallowing).After ethical committee approval,
informed written consent will be obtained from all patients.
Consenting patients scheduled to have hypospadias surgery will be randomised to sacral
erector spinae block or caudal block at the begin of surgery.
All patients heart rate,MAP and Oxygen saturation record intraoperatively. All patients will
receive paracetamol if requirement for postoperative analgesia.All patient will transfer from
PACU to day-surgery unit (DSU) if they achieved Modified Aldrete Score of ten.
All patients will be assessed postoperatively by a blinded investigator: in the
postanesthesia care unit and at 30 min 1,2, 4, 6, 12, 24, hour postoperatively.FLACC score
will be used.
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