About this trial
The goal of our study is to compare ultrasound-guided caudal block to the conventional technique based on anatomical landmarks.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
children aged between 6 months and 6 years, ASA 1 , underwent elective surgery
Disqualifiers
severe systemic diseases, previous neurological or spinal disorders, coagulation abnormalities, allergies toward LAs, local infection at the block site
Trial design
Parallel
Treatments tested in this trial
Ultrasound guided caudal Block
Procedure/Surgerycaudal block using Ultrasound
Conventionel
Procedure/SurgeryCaudal Block based on anatomical landmarks
Treatment groups
Trial outcomes
Primary outcomes
Success rate of block
A successful block was defined as an absence of significant motor movements following surgical induction or aberrations in the heart or respiratory rates
Secondary outcomes
block performing time
the period between anatomical structures identification and termination of LA administration
number of needle puncture
complication rates
Blood aspiration Subcutaneous bulging Bone contact Dural puncture Local anesthetic toxicity
Sponsors and contacts
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