The purpose of this study is to determine whether the use of the Epidrum device to identify the epidural space in labouring parturients reduces morbidity, when compared to standard loss of resistance techniques.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
300
Epidrum is used
National Maternity Hospital
Dublin, Co Dublin, Ireland
RATE OF OCCURRENCE OF DURAL PUNCTURE
Time frame: FIRST 48 HRS
RATE OF EPIDURAL BLOOD PATCH
Time frame: I MONTH AFTER LAST PATIENT RECRUITED
RATE OF EPIDURAL FAILURE REQUIRING RE-SITING OF CATHETER
Time frame: 24 HOURS
RATE OF FAILURE IN IDENTIFYING EPIDURAL SPACE REQUIRING CHANGE OF OPERATOR
Time frame: 24
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