Labor Induction and Pain Relief With Paracetamol Versus Placebo
Status:
Not yet recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
Summary
Single-blind study conducted on 2 randomly selected groups of pregnant women carrying a
single fetus (from week 37 onward). One group will receive paracetamol 1 gr I.V. prior to
insertion of balloon catheter and the control group will receive 100 ml sodium chloride 0.9%
I.V prior to insertion of balloon catheter. An assessment of pain management will be
conducted using various assessment tools. additionally, mode of delivery and time from
catheter insertion to delivery will be assessed.