The primary outcome of this clinical trial is to compare the pain scores during labour and delivery of combined spinal epidural without intrathecal opioids and dural puncture epidural The secondary objective of this study is to compare the and fetomaternal outcomes
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
120
three labor analgesia techniques
three labor analgesia techniques
three labor analgesia techniques
Ain Shams University
Cairo, Abbasyia, Egypt
Elite Hospital
Kuwait City, Abbasyia, Kuwait
epidural Local anesthetic consumption
Time frame: 1 year
Maternal hypotension
maternal mean arterial blood pressure less than 50 mmhg
Time frame: 1 year
incidence of fetal bradycardia
a fetal heart rate of less than 100 beats per minute
Time frame: 1 year
incidence of maternal pruritus
Participants will be assessed for pruritus every hour, by grading the severity on a scale ranging from 0-3; 0 = none, 1 = mild, 2= moderate and 3 = severe
Time frame: 1 year
labour pain scores
Visual analogue scale with its 0 to 10 score range: (0 (no pain) to 10 ( Severe pain)
Time frame: 1 year
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